Medical Device Manufacturer · US , Palm Beach Gardens , FL

Biomet 3i, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2019
7
Total
7
Cleared
0
Denied

Biomet 3i, LLC has 7 FDA 510(k) cleared medical devices. Based in Palm Beach Gardens, US.

Latest FDA clearance: Jun 2025. Active since 2019. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Biomet 3i, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Michael Davis Quality and Regulatory Consulting, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Biomet 3i, LLC
7 devices
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