Medical Device Manufacturer · US , New York , NY

Overture Resurfacing, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023

Total

Cleared

Denied

Overture Resurfacing, Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.

Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Overture Resurfacing, Inc.

2 devices

1-2 of 2