Medical Device Manufacturer · US , Atlanta , GA

Vertera, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Vertera, Inc. has 2 FDA 510(k) cleared medical devices. Based in Atlanta, US.

Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Vertera, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vertera, Inc.

2 devices

1-2 of 2