Biomet 3i, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomet 3i, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Biomet 3i, Inc. has 13 FDA 510(k) cleared dental devices. Based in Palm Beach Gardens, US.
Historical record: 13 cleared submissions from 2007 to 2011.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biomet 3i, Inc.
13 devices
Cleared
Nov 18, 2011
OSSEOTITE 2 DENTAL IMPLANTS
Dental
200d
Cleared
Sep 01, 2011
ABUTMENTS FOR COMPETITIVE IMPLANT SYSTEMS-NOBEL REPLACE
Dental
185d
Cleared
Apr 01, 2011
OSSEOTITE II MODEL XIFOSSXXX
Dental
382d
Cleared
Mar 11, 2011
BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS - ENCODE ABUTMENTS
Dental
276d
Cleared
Mar 11, 2011
BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS-ENCODE ABUTMENTS
Dental
276d
Cleared
Dec 03, 2010
ENCODE PATIENT SPECIFIC ABUTMENT
Dental
120d
Cleared
Nov 08, 2010
CAM STRUCTSURE BARS
Dental
154d
Cleared
Nov 30, 2009
LOW PROFILE ABUTMENTS - INTERNAL AND EXTERNAL CONNECTION
Dental
118d
Cleared
Jul 21, 2008
CAM STRUCTSURE PRECISION MILLED BARS
Dental
115d
Cleared
Mar 07, 2008
CERTAIN CONTOURED MARGIN CERAMIC ABUTMENT
Dental
100d
Cleared
Jan 31, 2008
NANOTITE PREVAIL,CERTAIN,PARELLEL WALLED,TAPERED,EXTERNAL HEX
Dental
161d
Cleared
Dec 20, 2007
BIOMET 3I DENTAL ABUTMENTS AND RESTORATIVE COMPONENTS
Dental
93d
Cleared
Aug 30, 2007
QUICKBRIDGE TM CYLINDER AND CAP
Dental
85d