ZetrOZ Systems Reports Wearable Ultrasound Device, SAM, Receives Expanded FDA Re-Approval: Positioning the Company for Market Growth in 2021

December 29, 2020

ZetrOZ Systems, developers of the Sustained Acoustic Medicine (SAM) wearable ultrasound, an FDA-cleared bio regenerative medical device, is the global leader in development of SAM technologies.

With its reapproval for expanded use in 2020, the use of SAM ultrasound technology in both professional and at-home applications is expected to increase market growth significantly over the next several years.

Video here.

“The benefits of SAM are growing clearer by the day as more research-based evidence becomes available supporting SAM’s ability to provide healing relief without surgery,” according to Dr. George Lewis, Founder and CEO of ZetrOZ. “More professional athletic organizations and sports medicine doctors are taking notice, and we hope that more people will come to learn about the deep healing relief that SAM technology can provide.”

SAM technology is backed by tens of millions of dollars from the National Institutes of Health (NIH) and Department of Defense (DoD) for its ability to treat pain without surgery or opioids. The use of SAM is being integrated into clinical training with plans to expand into commercial insurance markets to treat patients; over 300,000 patients have been treated across government agencies, including Veterans Affairs, DoD, and Department of Labor (DoL), and the private sector.

Multiple studies are always underway to increase the knowledge of SAM in sports medicine, pain management, and rheumatology. In addition to research on SAM products, ZetrOZ is developing a pipeline of additional bioelectronic devices to improve healthcare and society. ZetrOZ has a vision to help 100 Million patients suffering from chronic pain and soft-tissue injuries.

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”