Medical Device Manufacturer · US , Huntington Beach , CA

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

4 submissions · 4 cleared · Since 1993

Total

Cleared

Denied

Armm, Inc. has 4 FDA 510(k) cleared medical devices. Based in Huntington Beach, US.

Historical record: 4 cleared submissions from 1993 to 1998. Primary specialty: General & Plastic Surgery.

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

4 devices

1–4 of 4