Medical Device Manufacturer · US , Oakland , TN

Plexus Biomedical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2011

1

Total

0

Cleared

1

Denied

Plexus Biomedical, Inc. has 0 FDA 510(k) cleared medical devices. Based in Oakland, US.

Active since 2011. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) Regulatory Record - Plexus Biomedical, Inc.

1 devices

1-1 of 1

Not Cleared Jan 13, 2011

HEM-AVERT PERIANAL STABILIZER

DEN090011 · OOA

Obstetrics & Gynecology · 513d