Medical Device Manufacturer · US , Santa Barbara , CA

Aibiomed, Corp. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2018

1

Total

0

Cleared

1

Denied

Aibiomed, Corp. has 0 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.

Active since 2018. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Aibiomed, Corp.

1 devices

1-1 of 1

Not Cleared Nov 02, 2018

Parathyroid Detection (Model PTeye) System

DEN170056 · QDF

General & Plastic Surgery · 403d