Biomet Manufacturing, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomet Manufacturing, Inc. - FDA 510(k) Cleared Devices
Recent clearances: COMPREHENSIVE CONVERTIBLE GLENOID, METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS, COMPREHENSIVE REVERSE SHOULDER
32
Total
32
Cleared
0
Denied
Biomet Manufacturing, Inc. has 32 FDA 510(k) cleared orthopedic devices. Based in Warsaw, US.
Historical record: 32 cleared submissions from 1999 to 2013.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biomet Manufacturing, Inc.
32 devices
Cleared
Oct 09, 2013
COMPREHENSIVE CONVERTIBLE GLENOID
Orthopedic
236d
Cleared
May 18, 2012
METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS
Orthopedic
196d
Cleared
Dec 16, 2011
COMPREHENSIVE REVERSE SHOULDER
Orthopedic
56d
Cleared
Aug 15, 2008
HIPLOC COMPRESSION HIP SCREW
Orthopedic
157d
Cleared
Jun 11, 2008
BIOMET SPORTS MEDICINE ANCHOR DEVICES AND ZIPLOOP CONSTRUCTS
Orthopedic
149d
Cleared
Oct 23, 2007
BIOMET CABLE SYSTEM
Orthopedic
169d
Cleared
May 04, 2007
100KGY E-POLY ACETABULAR LINERS-ADDITIONAL PROFILES
Orthopedic
81d
Cleared
Feb 02, 2007
TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II...
Orthopedic
73d
Cleared
Sep 25, 2006
23 MM SINGLE-PEG PATELLA COMPONENT
Orthopedic
133d
Cleared
Aug 21, 2006
VANGUARD ANATOMIC PATELLA GROOVE (APG) / VANGUARD V GROOVE
Orthopedic
89d
Cleared
Aug 14, 2006
REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS
Orthopedic
241d
Cleared
May 03, 2006
GENERATION 4 POLISHED FEMORAL HIP PROSTHESIS WITH PROXIMAL CEMENT SPACER
Orthopedic
219d