Biomet Orthopedics FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Comprehensive Reverse Shoulder - HA Glenosphere Baseplates510(k)Apr 15, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Apr 15, 2026
A.L.P.S. Small Fragment Plating System510(k)Feb 19, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Feb 19, 2025
Comprehensive Segmental Revision System(SRS)510(k)Jul 12, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jul 12, 2023