Medical Device Manufacturer · US , Vista , CA

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

27 submissions · 27 cleared · Since 2005

27

Total

27

Cleared

0

Denied

Seaspine, Inc. has 27 FDA 510(k) cleared medical devices. Based in Vista, US.

Last cleared in 2023. Active since 2005.

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

FDA 510(k) cleared devices by Seaspine, Inc.

1 devices

1-1 of 1

Cleared Aug 03, 2023

NorthStar OCT System

Orthopedic · 58d