Erbe Elektromedizin GmbH - FDA 510(k) Cleared Devices

Erbe Elektromedizin GmbH has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Orange, US.

Latest FDA clearance: Jun 2026. Active since 1994.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

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