Erbe USA, Inc. - FDA 510(k) Cleared Devices

Erbe USA, Inc. has 39 FDA 510(k) cleared medical devices. Based in Lawrenceville, US.

Last cleared in 2022. Active since 1994. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.