Biomet Manufactuting Corp. is one of 18555 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomet Manufactuting Corp. - FDA 510(k) Cleared Devices
Recent clearances: G7 Finned Acetabular Shell, COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM
2
Total
2
Cleared
0
Denied
Biomet Manufactuting Corp. has 2 FDA 510(k) cleared medical devices. Based in Warsaw, US.
Historical record: 2 cleared submissions from 2012 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Biomet Manufactuting Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biomet UK, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Biomet Manufactuting Corp.
2 devices