Biomet 3i, Inc.
Biomet 3i, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2011.
Top product codes for Biomet 3i, Inc.
Recent clearances by Biomet 3i, Inc.
- K111216 — OSSEOTITE 2 DENTAL IMPLANTS
- K110565 — ABUTMENTS FOR COMPETITIVE IMPLANT SYSTEMS-NOBEL REPLACE
- K100724 — OSSEOTITE II MODEL XIFOSSXXX
- K101607 — BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS - ENCODE ABUTMENTS
- K101608 — BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS-ENCODE ABUTMENTS
- K102209 — ENCODE PATIENT SPECIFIC ABUTMENT
- K101582 — CAM STRUCTSURE BARS
- K092341 — LOW PROFILE ABUTMENTS - INTERNAL AND EXTERNAL CONNECTION
- K080864 — CAM STRUCTSURE PRECISION MILLED BARS
- K073345 — CERTAIN CONTOURED MARGIN CERAMIC ABUTMENT
- K072363 — NANOTITE PREVAIL,CERTAIN,PARELLEL WALLED,TAPERED,EXTERNAL HEX
- K072642 — BIOMET 3I DENTAL ABUTMENTS AND RESTORATIVE COMPONENTS
- K071551 — QUICKBRIDGE TM CYLINDER AND CAP
Data sourced from openFDA. This site is unofficial and independent of the FDA.