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PRNews

Frost & Sullivan Acclaims Shimadzu for Delivering a Product Line of Versatile and Innovative Radiography Solutions

Shimadzu’s products utilize advanced robotic capabilities and next-generation digital imaging technologies

LONDON, Aug. 3, 2017 /PRNewswire/ — Based on its recent analysis of the general radiography market, Frost & Sullivan recognizes Shimadzu Corporation with the 2017 Global Frost & Sullivan Award for Product Line Strategy Leadership. Constant innovations and upgrades to Shimadzu’s radiography product portfolio have ensured that the products stay relevant and in high demand in an evolving radiography market. Its comprehensive product range enhances automation, efficiency, image quality, and overall clinical value by enabling flexible positioning, reduced radiation dose, and versatility in viewing bone and soft tissue images.

Shimadzu has the entire range of general radiography solutions, from fixed ceiling-mounted to floor-mounted systems and mobile X-ray solutions, with or without one to two arms. These are all available all in entry-level to high-end configurations. In 2016, it introduced new technologies such as digital multi-slice tomography with flexible positioning to offer a view of oblique cross sections of the spine and hip joints. Other products include:

  • SONIALVISION G4, a fluoroscopy product with multi-functionality features
  • RADspeed Pro EDGE package, a high-performance general radiography equipment
  • MobileDaRt Evolution MX7 Version, mobile X-ray with digitization features.

RADspeed Pro EDGE and MobileDaRt Evolution MX7 have already been adopted by more than 100 hospitals worldwide within a year of their introduction.

“In response to customer demand, Shimadzu introduced a sophisticated, remote-controlled, auto-positioning feature in the RADspeed Pro EDGE package. This feature helps the radiographer effortlessly position the tube and fine-tune this positioning to improve patient safety and reduce radiation dose,” said Frost & Sullivan Consultant Poornima Srinivasan. “Similarly, it incorporated removable grids to lower radiation exposure during pediatric imaging, and a dose area product meter on the collimator to measure the dose of radiation the patient is exposed to.”

Shimadzu’s products have proven their utility in guiding hospitals towards the era of value-based healthcare. They achieve that by incorporating a host of novel features and technologies.

  • The RADspeed Pro EDGE employs cutting-edge technologies like tomosynthesis, speed stitch, and dual energy subtraction. Tomosynthesis combines cone-beam computed tomography (CT) reconstruction with digital image processing so that any number of cross-sectional images can be obtained. The systems also incorporate ‘T-smart,’ the metal artifact reduction technology that decreases metal artifacts in orthopedic patients. Additionally, it uses speed stitch technology, which combines multiple images that are captured while the X-ray tube is in motion at various angles. Finally, its dual energy subtraction, imaging algorithm, couples with low and high voltages to offer images of soft tissue and bone images separately.
  • SONIALVISION G4 is capable of a wide range of examinations and is ideal for inter-departmental shared services. The field of view (FOV) flat panel detector (FPD) is available in five sizes and provides an extensive imaging area, ultra-high definition and dynamic images, less radiation exposure, a ceiling-mounted telescopic arm, and a wall stand with a portable FPD. It incorporates technologies such as:
    • The SUREengine-Advance, an image processing technology that delivers quality fluoro and radiography images
    • SLOT Advance, an optimal technology for long-view images with a minimal X-ray dose
    • T-smart, the latest tomosynthesis technology that aids in iterative reconstruction with metal artifact suppression
  • The MobileDaRt Evolution MX7 Version incorporates a large LCD monitor and LED collimator light that increases brightness up to 40% and saves electricity by 80% when compared to its competing products. It also has a user-friendly design with wireless capability, which allows it to extend its scope of application.

“Shimadzu has leveraged the expertise of key opinion leaders (KOLs), designed training and educational programs, expanded geographically, and made the most of cross-selling opportunities in line with its business goals,” noted Ms. Srinivasan. “Additionally, it has partnered with universities to optimize the existing systems and develop further innovations and efficiencies. Shimadzu’s discussions with international channels, and focus on gathering input from healthcare professionals have played a huge role in its development of unique products and provision of a rich customer experience.”

Each year, Frost & Sullivan presents this award to the company that has developed a comprehensive product line that caters to the breadth of the market it serves. The award recognizes the extent to which the product line meets customer base demands, the overall impact it has in terms of customer value, as well as increased market share.

Frost & Sullivan Best Practices awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

About Shimadzu Corporation

Shimadzu Corporation has remained committed to commercializing cutting-edge technology and providing it to customers in a wide array of industries for more than 140 years. Our brand statement, “Excellence in Science”, reflects our desire and attitude to diligently respond to customers’ requirements by offering superior, world-class technologies indispensable for analytical and measuring instruments, medical systems, aircraft equipment and industrial machinery in the area of human health, safety and security of society and advancement of industry. In the ever-changing landscape of challenges of society, Shimadzu aims to partner with customers to meet their needs with unique technologies and solutions.

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, works in collaboration with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, we have been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

Contact:

Ana Arriaga
P: 210.247.3823
F: 210.348.1003
E: ana.arriaga@frost.com

PRNews

OrthoAccel Technologies, Inc. Names Orthodontic and Dental Industry Executive David Josza as CEO

HOUSTON, July 26, 2017 /PRNewswire/ — OrthoAccel® Technologies, Inc. announces that its board of directors has named David Josza, an orthodontic and dental industry senior executive with more than 25 years of experience, as CEO effective August 1, 2017. A privately owned medical technology start-up, OrthoAccel recently launched its third-generation vibratory orthodontic device AcceleDent® Optima™ that enables orthodontists to achieve more predictable outcomes. AcceleDent Optima is an FDA-cleared, Class II medical device that is clinically shown in randomized control trials to speed up orthodontic treatment by as much as 50 percent while reducing discomfort by up to 71 percent during treatment.

“OrthoAccel is a market leader in accelerated orthodontic technology and I am delighted to lead the company’s next phase of growth and innovation,” said Josza. “This is an exciting stage in OrthoAccel’s trajectory and, based on the feedback of orthodontists and patients who have experienced the new AcceleDent Optima, there is significant opportunity for growth ahead for this best-in-class treatment technology.”

Josza most recently served as corporate vice president and general manager for Zimmer Biomet Dental, a leading global manufacturer of musculoskeletal devices. He joined Zimmer in 2015 when the company acquired his previous firm, Biomet, Inc., and Josza was tapped to lead the complex acquisition integration. Among his accomplishments, he successfully implemented synergistic cost-saving initiatives and cross-selling opportunities that yielded significant profit increases and growth.

Prior to the acquisition, Josza had a 14-year career at Biomet 3i, a global implant and oral reconstructive supplier, most recently serving as vice president of the Americas. As a member of the executive board, he was responsible for developing and delivering the company’s annual strategic plan.

Additional accomplishments at Biomet included developing and leading a variety of significant revenue growth initiatives, including capturing the market leader position in Latin America. Another key accomplishment was the commercialization of a new digital product line, with a specialized sales team and a technical service support function that grew incremental revenue by $2 million in its first year.

In addition to his leadership roles at Zimmer and Biomet, Josza’s in-depth experience includes previous business development, strategic planning and management responsibilities at Henry Schein, Inc. and Stryker Corporation.  

“We are excited to welcome David and recognize that his in-depth experience in dental and medical industries, combined with his many successes as a strategist and business developer, provide an excellent leadership platform for his role at OrthoAccel Technologies,” said Brian R. Smith, chairman of OrthoAccel’s board of directors and managing director of S3Ventures.

The leader in accelerated orthodontics, OrthoAccel has received numerous business and medical design awards that reflect the company’s success in commercializing its patented SoftPulse Technology® for clinical application. AcceleDent has been recognized as the preferred accelerated orthodontic treatment solution by orthodontists participating in surveys conducted by industry journals Orthotown and the Journal of Clinical Orthodontics.

For more information about OrthoAccel and the company’s innovative orthodontic solutions, visit AcceleDent.com.

About OrthoAccel® Technologies, Inc.
OrthoAccel® Technologies, Inc. is a privately owned medical device company engaged in the creation, manufacturing, marketing and sales of innovative solutions that enhance dental care and orthodontic treatment. Among the company’s innovations is AcceleDent® Optima™, an FDA-cleared, Class II medical device that employs patented SoftPulse Technology® that is demonstrated to speed up bone remodeling. These safe and gentle vibrations accelerate tooth movement by as much as 50 percent and reduce discomfort associated with orthodontic treatment by up to 71 percent. Leading orthodontists from around the world report increased mechanical efficiency with orthodontic appliances and improved predictability of clinical outcomes with AcceleDent.  OrthoAccel, the Leader in Accelerated Orthodontics, is ranked on Deloitte’s 2016 Technology Fast 500 as one of the fastest growing companies in North America. OrthoAccel is based in Houston, Texas and maintains a global presence through its EMEA office in Essen, Germany. To learn more about OrthoAccel’s focus on improving the journey to healthy, beautiful smiles, visit AcceleDent.com.

Source: OrthoAccel Technologies, Inc.

PRNews

Frost & Sullivan Acclaims CGI’s Advanced Genomic & Biomarker Technologies That Drive Industry Innovation in Support of Precision Cancer Treatment

CGI’s technologies provide valuable insights across cancer diagnostics through the accurate and sensitive quantitation of clinically relevant genomic signatures & biomarkers from both blood and tissue samples

SANTA CLARA, California, July 26, 2017 /PRNewswire/ — Based on its recent analysis of the precision oncology industry, Frost & Sullivan recognizes Cancer Genetics, Inc. (CGI or the Company) with the 2017 North American Frost & Sullivan Award for Technology Innovation. CGI’s leading-edge technology platforms and comprehensive menu of diagnostic services enhance precision oncology by enabling earlier cancer detection, improving treatment management, and aiding the development of novel cancer therapies. The Company’s genomic products and services not only present diagnostic, prognostic, and theranostic information for routine clinical care, but also facilitate and accelerate drug development programs seeking to deliver targeted, more effective and safer drugs to market more quickly. With its comprehensive suite of both off-the-shelf and proprietary tests, technology-agnostic approach, global infrastructure, and extensive research collaborations, CGI is at the forefront of enabling precision medicine in oncology globally, from bench to bedside.

“CGI has a wide variety of assays for genomic and immuno-oncology related biomarkers, applicable across several therapeutic areas, including hematological malignancies, solid tumors, and hereditary cancers,” said Frost & Sullivan Research Analyst Vandana Iyer. “The Company offers a broad range of laboratory services that provide critical genomic and biomarker information for patient care and for clinical trials being performed by biotech and pharmaceutical companies. CGI’s recent launches of cutting edge tests, its ability to partner with innovative companies, and its extensive research collaborations with leading academic institutions and cancer centers are a testament to the value and depth of CGI’s commitment to driving industry innovation.”

Some of CGI’s prominent and recently launched technologies include:

  • Complete::IO™ is a unique and in-depth flow cytometry panel supporting informed therapeutic decisions and assessment of potential toxicities for novel immuno-oncology (IO) therapies in blood cancers and solid tumors.
  • Focus::Oncomine™ is capable of simultaneously testing DNA and RNA, enabling the detection of various types of genomic alterations in a single workflow that requires minimal sample quantities and boasts a rapid turnaround time. The Focus::Oncomine™ assay can detect thousands of clinically and pharmacologically relevant biomarkers in solid tumors, making it a valuable tool for clinicians and biopharma.
  • Focus::Lymphoma™ is the most comprehensive next generation sequencing (NGS) panel for B-cell lymphomas in the field.  Focus::Lymphoma™, sequences 220 clinically-actionable genes, allowing clinicians to determine the most effective treatment management for patients. Focus::Lymphoma™ is also offered to biotech and pharmaceutical companies to power efficient clinical trials focused on B-cell lymphomas.
  • Focus::Renal™ is a highly-sensitive NGS panel that provides thorough information for the diagnosis, prognosis and therapy selection in renal cancers.  In a single test, Focus::Renal™ is able to detect mutations in 76 renal cancer-related genes, as well as genome-wide copy number changes, and critical single nucleotide polymorphisms (SNPs). Focus::Renal™ is the only NGS panel of its type, as it is disease-focused, and has been developed through collaboration with leading cancer centers and academic institutions, including MSKCC, Cleveland Clinic, Huntsman Cancer Center at University of Utah, and University Hospital of Paris.
  • Liquid::Lung-cfDNA™ is a CLIA-validated, multi-gene NGS panel for lung cancer liquid biopsies. The test can detect lung tumor-derived cell-free DNA (cfDNA) obtained from a single blood draw, and analyzes frequently-mutated SNPs and short indels in 11 genes with significant clinical relevance to non-small cell lung cancer (NSCLC). This groundbreaking assay is highly sensitive, with a limit of detection (LOD) as low as 0.05% or 1 mutant copy of DNA in a background of 2,000 wild-type copies of DNA.
  • Focus::HERSite™ is a hereditary cancer test that focuses on breast and ovarian cancers. The test analyzes the 16 genes most commonly associated with breast and ovarian cancers and provides in-depth coverage of BRCA1 and BRCA2.
  • Oncomine Dx Target Test is the first NGS-based companion diagnostic (CDx) test that simultaneously screens tumor samples for biomarkers associated with 3 FDA-approved therapies for non-small cell lung cancer (NSCLC). CGI is one of the first laboratories, and one of only three in the United States, to offer the Oncomine Dx Target Test.

CGI has established a global footprint with a presence in the United States, India, and China. The Company’s infrastructure, which has been developed through strategic acquisitions, and its unique business model, which incorporates routine clinical testing for cancer patients and fee-for-service solutions for biotech and pharmaceutical companies, have positioned it uniquely for diversified growth and access to the oncology community. These factors have supported the Company’s successful development of a durable business model through which to commercialize its oncology programs and testing capabilities.

“CGI is a technology-agnostic company with comprehensive diagnostic capabilities utilizing various platforms, including next generation sequencing, fluorescence in situ hybridization, immunohistochemistry, microarrays, RT-PCR, and flow cytometry. The Company boasts full NGS capabilities with both Illumina and Thermo Fisher platforms, offering a mix of proprietary panels and off-the-shelf assays,” noted Iyer. “CGI has several ongoing research collaborations with leading oncologists and cancer centers in both solid tumors and hematological malignancies, including kidney cancer, leukemia, non-Hodgkin’s lymphoma, and HPV-associated cancers. The Company constantly strives for diversity and innovation, and has successfully achieved a balance between the two.”

Each year, Frost & Sullivan presents this award to the company that has demonstrated uniqueness in developing and leveraging new technologies, which significantly impact both the functionality and the customer value of new products and applications. The award lauds the high R&D spend towards innovation, its relevance to the industry, and the positive impact on brand perception.

Frost & Sullivan Best Practices awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

ABOUT CANCER GENETICS, INC.

Cancer Genetics, Inc. is a leader in enabling precision medicine in oncology from bench to bedside through the use of oncology biomarkers and molecular testing. CGI is developing a global footprint with locations in the US, India and China. We have established strong clinical research collaborations with major cancer centers such as Memorial Sloan Kettering, The Cleveland Clinic, Mayo Clinic, Keck School of Medicine at USC and the National Cancer Institute.
The Company offers a comprehensive range of laboratory services that provide critical genomic and biomarker information. Its state-of-the-art reference labs are CLIA-certified and CAP-accredited in the US and have licensure from several states including New York State.

For more information, please visit or follow CGI at:

Internet: www.cancergenetics.com
Twitter: @Cancer_Genetics
Facebook: www.facebook.com/CancerGenetics
Media Contact:
Panna Sharma
Cancer Genetics, Inc.
Tel: 201-528-9200
Email: panna.sharma@cgix.com

Investor Relations Contact:
Richard Moyer
Cameron Associates
535 Fifth Ave., New York, NY 10017
Tel: 212-554-5466
Email: richard@cameronassoc.com

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, works in collaboration with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, we have been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

Contact:

Andrea Steinman
P: 210.477.8425
F: 210.348.1003
E: andrea.steinman@frost.com

PRNews

Early Treatment Is Revolutionizing Outcome Of Burn Scars

Lasers are improving severe scars and pain in Military personnel and burn victims

BURLINGTON, Massachusetts, July 25, 2017 /PRNewswire/ — Early treatment of burn scars with lasers is revolutionizing the outcome of many burn and trauma scar patients. In the past, doctors were taught to wait at least a year before treating burn and trauma scars, but according to Jill Waibel, MD, “That’s really counterintuitive, because the scars get worse. These patients can have horrific, disfiguring, painful contracture scars that form and a lot of our patients are children. We’ve seen that when you go in early, they need less surgery and less laser treatment.”

Laser devices, such as the Lutronic eCO2 laser, originally designed to treat wrinkles and acne scars, are found to have the capability to also improve disfiguring burn scars and other scars, as well as significantly reduce pain in these patients. Jill S. Waibel, MD, world renown Dermatologist, recently completed a clinical trial with Lutronic Aesthetics, proving early scar treatment with lasers is successful and she has been using this approach in practice and with her work on military personnel with battle scars for the last four to five years. Dr. Waibel has also helped many children and people of all ages with burn scars, surgery scars and scars of all types and shares her knowledge with other physicians around the globe.

“I believe we were the first to treat a burn survivor with fractional ablative CO2 in 2011. This is the first randomized control study in severe trauma patients to show early intervention with the Lutronic eCO2 prevents scarring when used within the first 3 months after burn injury. This information could potentially help patients live a better quality of life.” Jill S. Waibel, MD

Dr. Waibel will be discussing the topic “Early Intervention – New Paradigm in Treatment of Burn Scars” in a live Webinar on July 27th. For more information or to register, please visit www.usa.lutronic.com.

About Lutronic 
Lutronic, a leading innovator in advanced aesthetic and medical laser technology, was established over 19 years ago to bring state-of-the-art innovative, yet affordable devices to the worldwide aesthetic community.  All systems optimize outcomes for a wide variety of conditions and treatments including melasma, burn scars, tattoo removal, vascular lesions, hair removal, wrinkle reduction, rejuvenation, body/face contouring, chronic pain, healing and more.

Devoting more than 20% of revenue to R&D, Lutronic holds more than 200 current and pending patents worldwide. With more than 270 employees worldwide, Lutronic has offices in the US, Korea, China and Japan, a world-wide network of distributors and a focused R&D center in Korea.

For more information about LUTRONIC, visit: www.lutronic.com

If you would like more information about this topic, please contact Rachel Deschamps at 603-560-5103 or email at rdeschamps@lutronic.com.

Contact

Rachel Deschamps

Cell

603-560-5103

Email

rdeschamps@lutronic.com

Website

www.usa.lutronic.com
PRNews

U.S. FDA Determines Celliant (R) Responsive Textile Products Meet Criteria as Medical Devices and General Wellness Products

– Hologenix, LLC’s technology is first of its kind to secure joint FDA designations 

– Celliant-engineered products clinically proven to promote increased localized blood flow

– FDA determination to usher in new era of performance fabrics, responsive textiles

LOS ANGELES, July 25, 2017 /PRNewswire/ — Hologenix, LLC, maker of Celliant, the world’s most advanced, clinically tested responsive textile technology, announced today that the U.S. Food and Drug Administration (FDA) has determined Celliant products are medical devices and general wellness products, as defined in Section 201(h) of the Federal Food, Drug and, Cosmetic Act. According to the FDA, Celliant products were determined to be medical devices because they temporarily promote increased local blood flow at the site of application in healthy individuals.


PureCare Elements: Lumen® Premium Celliant® Sheet Set: The first linen collection that uses Celliant to increase comfort and promote faster recovery while you sleep.

SIMA award winner, Xcel Infinity Comp TDC Full Suit with Celliant: Uses Celliant to create the warmest wetsuit lining so you can surf longer and recover faster.

ISPO award winner, Tecnica Mach 1 Pro Women Ski Boot: A ski boot made for women by women that uses Celliant and Lambswool Heat from Imbotex in its lining to address women’s specific needs for warmth, comfort and performance on and off the slope. Release date: Fall 2017

Salewa Puez TirolWool Celliant Half Zip Jacket: Bends TirolWool, naturally warm, breathable and hydrophobic insulation from Imbotex, with Celliant to keep outdoor enthusiasts energized and warm all day long. Release date: Fall 2017

“Celliant-engineered products are the first of their kind that the FDA has designated as medical devices,” said Seth Casden, Hologenix CEO. “Our technology can be used in everyday products — t-shirts, clothing, bedding, even airplane seats — to create an increase in local blood flow thereby increasing energy, boosting performance and speeding muscle recovery.”

“We believe that Celliant is a truly disruptive technology that has transformational applications for textiles,” Casden said. “We’re currently evaluating additional applications of Celliant in the healthcare space, where, for example, people who suffer from diabetes might benefit from increased blood flow to body tissue.”

Celliant-engineered products harness and recycle the natural heat emitted by human beings to boost performance and rebuild and recharge the human body after physical activity and while you sleep. Celliant is made of a patented blend of thermo-reactive minerals infused into the core of fiber used to create all types of textiles and fabrics so it does not wash or wear out. Products made with Celliant fabric absorb and convert body heat into infrared energy (IR) that is recycled back into skin and tissue in a safe, natural way. IR is a vasodilator, increasing blood flow to tissue and muscles throughout the body, which delivers vital nutrients and oxygen to the cells. The effect is clinically proven to help the body:

  • increase energy, endurance, stamina and performance,
  • recover faster from physical activity,
  • promote restful sleep and increased comfort.

Celliant is used in a diverse range of textiles and applications – apparel, bedding, wetsuits and veterinary products, including:

  • SIMA award winner, Xcel Infinity Comp TDC Full Suit with Celliant which uses Celliant to create the warmest wetsuit lining so you can surf longer and recover faster;
  • Salewa Puez TirolWool Celliant Half Zip Jacket that blends TirolWool, naturally warm, breathable and hydrophobic insulation from Imbotex, with Celliant to keep outdoor enthusiasts energized and warm all day long. Release date: Fall 2017;
  • ISPO award winner, Tecnica Mach 1 Pro Women Ski Boot, a ski boot made for women by women that uses Celliant and Lambswool Heat from Imbotex in its lining to address women’s specific needs for warmth, comfort and performance on and off the slope. Release date: Fall 2017;
  • PureCare Elements: Lumen® Premium Celliant® Sheet Set, the first linen collection that uses Celliant to increase comfort and promote faster recovery while you sleep.

“Science has shown that infrared energy increases blood flow, improves muscle recovery and reduces long-term pain,” said Dr. Michael R Hamblin, principal investigator at the Wellman Center for Photomedicine at Massachusetts General Hospital. “The FDA’s determination of Celliant products as medical devices and general wellness products will likely spur interest in infrared technologies and further development of garments and wraps that can positively impact people’s well-being.”

Celliant has been extensively researched, developed and clinically tested for both durability and effectiveness. Prominent institutions have conducted nine clinical trials to evaluate Celliant’s performance including University of California Irvine, University of Calgary, UCI Long Beach Veterans Affairs Medical Center, Texas A&M University, Loyola University Chicago and Exponent. Celliant technology has been shown to increase tissue oxygen levels by eight percent at the site of applicationi. Click here for NIH independent study on the benefits of IR on recovery.

About Celliant®
Celliant is a revolutionary, patented technology that harnesses and recycles the body’s natural energy through the medium of fibers. Celliant’s applied science utilizes a blend of minerals and proprietary ingredients that are embedded into the core of the fiber. Use of products containing this technology has been clinically proven to enhance tissue oxygen levels, improve athletic performance, sleep quality, health and wellness. Fibers, yarns and fabrics with Celliant technology can be found in some of the world’s most recognized name brands. For more information, visit www.celliant.com.  

About Hologenix, LLC
Founded in 2002, Hologenix, LLC, maker of Celliant technology, is committed to creating, developing and bringing to market products that enhance people’s lives through new materials. They strive to deliver the future of healthy innovation through a variety of consumer categories. In addition to the United States, Celliant is designated as a Class I medical device in Canada, European Union, Australia and New Zealand. The Company continues to explore new territories and is currently running FDA-focused, clinical trials to expand into the medical product arena.

i Dr. Ian Gordon – University of CA, Irvine, Effect of Garment with 42% Celliant Fiber on TCP02 Levels and Grip Strength in Healthy Subjects. 2010

Contact: Julia Moore, +1-212-445-8160, Julia.Moore@webershandwick.com

Photo – http://mma.prnewswire.com/media/538683/PureCare_Sheets.jpg
Photo – http://mma.prnewswire.com/media/538684/Xcel_Infinity_Comp_Full_Suit.jpg
Photo – http://mma.prnewswire.com/media/538685/Tecnica_Mach_1_Pro_Women_Ski_Boot.jpg
Photo – http://mma.prnewswire.com/media/538686/Salewa_Puez_TirolWool_Celliant_Half_Zip_Jacket.jpg
Logo – http://mma.prnewswire.com/media/538687/Celliant_Logo.jpg 

PRNews

MyDx Files Complaint Against Former Chief Operating Officer, Protects Unique AeroDx Diagnostic Platform and Addresses Toxic Financier’s Unauthorized Conversion

SAN DIEGO, July 18, 2017 /PRNewswire/ — MyDx, Inc. (OTCQB:MYDX), a science and technology company and creator of MyDx® (My Diagnostic), the first multi-use handheld chemical analyzer initially designed for cannabis professionals and retail consumers to measure the chemicals in cannabis and track their feedback on how each sample is impacting their physiology, today announced that all previously reported variable toxic debts have been satisfied through the unauthorized conversion of the Crown Bridge note and has also filed a lawsuit against its former COO and other defendants who have attempted to create a competitive advantage with its anticipated product launch of its air quality sensor: AeroDx®.


MyDx 2.0 Analyzer with CannaDx and AeroDx Sensor Compatibility

Lawsuit to Protect Unique AeroDx Diagnostic Platform
On July 14, 2017, the Company and its Chief Executive Officer, Daniel Yazbeck, filed a complaint in Superior Court of California against a series of Defendants who have allegedly engaged in unfair business practices, made false statements about the Company, its products, and Mr. Yazbeck at investor events and on online investor platforms.  There can be no assurance about the results or on the outcome of the lawsuit, however, the company took aggressive steps it felt were necessary to protect its business and its shareholders.

AeroDx®: MyDx’s Air Quality Sensor
AeroDx Sensors are the first of three anticipated versatile sensors to be launched into the market and represents the first versatile sensor to be used with the new release of the MyDx 2.0 Analyzer launched in May of this year.  AeroDx is expected to measure key air quality parameters for cannabis and non-cannabis consumers, to be interchanged seamlessly with the CannaDx Sensors. Once AeroDx Sensors are inserted into the MyDx Device, the device becomes an air quality tester with the ability to detect Volatile Organic Compounds (VOC’s) such as Formaldehyde, Butane, Toluene, Methane, Benzene and other harmful chemicals, such as Carbon Dioxide, present in the air. It can also monitor temperature and humidity, which can aid in preventing mold and germ growth. The company is also in the process of customizing the sensor in order to ensure air quality and control in cannabis growth facilities as well offer a test for residual solvents in cannabis oils.

Addressing Remaining Toxic Variable Convertible Debt on Balance Sheet
 On April 30, 2017, the Company sent a payoff demand to Crown Bridge Partners, LLC as required under the terms of the loan Agreement.  The Company agreed to repay, in full, the remaining variable toxic convertible note on its balance sheet prior to the prepayment deadline. Crown Bridge acknowledged the request and despite the Company and its counsel’s repeated payoff request, on July 3, 2017, Crown converted $36,749.04 (the entire amount due pursuant to the Note, including penalties and interest) into 14,699,616 shares of the Company’s common stock. In light of the Company’s notification and Crown Bridge’s acknowledgment required under the terms of the loan Agreements, Crown Bridge executed the conversion and the Company alleges it breached the terms of the Note. The Company will continue to evaluate its rights and determine the best course of action to advance the interests of its shareholders.

As of July 17, 2017, all previously reported variable rate toxic financing has been fully paid off.

About MyDx, Inc.
 MyDx, Inc. (OTCQB: MYDX) is a chemical detection and sensor technology company based in San Diego, California whose mission is to help people Trust & Verify® what they put into their minds and bodies. The Company developed MyDx®, a patented, affordable portable analyzer that provides real-time chemical analysis and fits in the palm of the user’s hand. The multi-use MyDx analyzer leverages over a decade of established chemical detection technology to measure chemicals of interest. The Company owns a substantial and growing intellectual property portfolio of patents covering its technology. The MyDx AquaDx®, OrganaDx(TM) and CannaDx(TM) sensors are now commercialized, and the AeroDx® application is next in line. All sensors will be compatible with a MyDx App that empowers consumers to live a healthier life by revealing the chemical composition of what they eat, drink and inhale. For more information, please visit www.mydxlife.com.

Forward-Looking Statements
This news release contains “forward-looking statements” as that term is defined in Section 27(a) of the Securities Act of 1933, as amended, and Section 21(e) of the Securities Exchange Act of 1934, as amended. Statements may contain certain forward-looking statements pertaining to future anticipated or projected plans, performance and developments, as well as other statements relating to future operations and results. Any statements in this press release that are not statements of historical fact may be considered to be forward-looking statements. Words such as “may,” “will,” “expect,” “believe,” “anticipate,” “estimate,” “intends,” “goal,” “objective,” “seek,” “attempt,” or variations of these or similar words, identify forward-looking statements. These forward-looking statements by their nature are estimates of future results only and involve substantial risks and uncertainties, including but not limited to risks associated with the uncertainty of future financial results, additional financing requirements, development of new products, our ability to complete our product testing and launch our product commercially, the acceptance of our product in the marketplace, the uncertainty of the laws and regulations relating to cannabis, the impact of competitive products or pricing, technological changes, the effect of economic conditions and other uncertainties detailed from time to time in our reports filed with the Securities and Exchange Commission, available at http://ir.cdxlife.com/all-sec-filings or www.sec.gov. MyDx is not considered a medical device.  Consumers should be advised that any claims regarding the medical benefits of cannabis are still under research and until approved by the FDA or any other relevant international regulatory body, are considered anecdotal in nature. 

Investor Contact:
MyDx Shareholder Communications
800.814.4550 ext. 4
ir@cdxlife.com

Photo – http://mma.prnewswire.com/media/536158/MyDx_Inc_Analyzer_with_CannaDx.jpg 

Source: MyDx, Inc.