FDA Clearance

FDA News Announces VERA's 510(k) Clearance for 'Rehabilitating the Trunk and Upper Extremities'

FDA News Announces VERA's 510(k) Clearance for 'Rehabilitating the Trunk and Upper Extremities'

The FDA News has now officially reported that we’ve received 510(k) clearance for the use of our VERA™ digital PT assistant for “rehabilitating the trunk and upper extremities,” an extension of our earlier FDA clearance for the treatment of lower extremities (i.e., knee and hip replacement surgery).

MobiHealthNews Discusses Our 510(k) Clearance for Trunk and Upper Extremities

MobiHealthNews Discusses Our 510(k) Clearance for Trunk and Upper Extremities

MobiHealthNews, a leading publication covering the latest trends and developments in digital healthcare, has published a report examining our recent 510(k) clearance from the FDA for the use of our Virtual Exercise Rehabilitation Assistant (VERA™) platform in the treatment of trunk and upper extremities.

Reflexion Health Digital Medicine Therapy Tool VERA Receives FDA 510(k) Clearance

San Diego, CA (November 3, 2015) – San Diego based Reflexion Health, a digital medicine company using Microsoft Kinect motion-tracking technology to re-imagine rehabilitation medicine; today announced the US Food and Drug Administration (FDA) has cleared its motion-tracking based physical therapy tool, Vera™.