Medical Device Manufacturer · US , St Augustine , FL

H&H Instruments - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1992

Total

Cleared

Denied

H&H Instruments has 2 FDA 510(k) cleared medical devices. Based in St Augustine, US.

Historical record: 2 cleared submissions from 1992 to 1992. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by H&H Instruments Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - H&H Instruments

2 devices

1-2 of 2