Medical Device Manufacturer · DE , Berlin

Aap Implantate AG - FDA 510(k) Cleared Devices

37 submissions · 37 cleared · Since 1999
37
Total
37
Cleared
0
Denied

Aap Implantate AG has 37 FDA 510(k) cleared orthopedic devices. Based in Berlin, DE.

Latest FDA clearance: Mar 2026. Active since 1999.

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

510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Aap Implantate AG
37 devices
1-12 of 37

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