Medical Device Manufacturer · US , Quakertow. , PA

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

4 submissions · 4 cleared · Since 2012

Total

Cleared

Denied

Oricare, Inc. has 4 FDA 510(k) cleared medical devices. Based in Quakertow., US.

Historical record: 4 cleared submissions from 2012 to 2014. Primary specialty: Anesthesiology.

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

4 devices

1–4 of 4