Medical Device Manufacturer · US , Apollo Beach , FL

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

2 submissions · 2 cleared · Since 2014

Total

Cleared

Denied

Kericure, Inc. has 2 FDA 510(k) cleared medical devices. Based in Apollo Beach, US.

Latest FDA clearance: Jul 2024. Active since 2014. Primary specialty: General & Plastic Surgery.

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

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

2 devices

1-2 of 2