Biomet, Inc.
Biomet, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 2026, with 255 FDA device recalls on record.
Clearances by Biomet, Inc. — page 5
401–442 of 442- K852584 — POROUS APF/COLLARLESS MODULAR FEMORAL COMPONENT
- K845025 — AUSTIN-MOORE MODULAR HIP PROSTHESIS
- K844941 — CFE ACETABULAR CUP
- K845005 — BROOKER ACETABULAR CUP
- K841437 — PENNSYLVANIA HOSPITAL HIP SYS
- K833921 — AGC TOTAL KNEE PROSTHESIS
- K833175 — BIOMET BIPOLAR PROSTHESIS
- K831512 — DOSIMETRY RELEASE OF RADIATION STERILIZ
- K831513 — KENNEDY TIBIAL COMPONENT
- K830314 — MILWAUKEE AUSTIN MOORE TOTAL HIP
- K830313 — CFE TOTAL HIP FEMORAL COMPONENT
- K830209 — LUS ACETABULAR COMPONENT
- K823059 — DOSIMETRY RELEASE OF RADIATION STERIL.
- K813581 — CRUCIATE LIGAMENT BUTTON
- K820539 — RELIEVED REINFORCED CUP
- K813089 — CEMENT RING
- K812946 — TRONZO HIP
- K811718 — SURFACE REPLACEMENT HIP PROSTHESIS
- K811738 — COLLARLESS TAPERED STEM HIP PROSTH. DEV
- K811223 — VASOVASOSTOMY STABILIZER PLATFORM DEV
- K810258 — PROXIMAL FERMORAL HIP REPLACEMENT
- K810120 — REINFORCED HIP CUP
- K800143 — DYNAMIC EXTENSOR SPLINT
- K800144 — FEMORAL CEMENT RESTRICTOR
- K790762 — PLATFORM TCCK TOTAL KNEE
- K780848 — PORTABLE CLOSED WOUND SUCTION EVACUATOR
- K781389 — BIOMET CONCENTRIC HEX SCREW
- K781294 — PROSTHESIS, KNEE, TOTAL
- K781091 — KNEE INSTRUMENTATION, CONDYLAR
- K780357 — TITANIUM MULLER TOTAL HIP
- K780227 — BANDAGE SPREADER BLOCK
- K780375 — PAVLIK HARNESS
- K780229 — ABDOMINAL BELT
- K780230 — BED BOARD
- K780225 — ORTHOSISES DEVICES
- K780228 — TRACTION UNITS
- K780233 — TRACTION WEIGHT BAGS
- K780234 — TRACTION BELT, PELVIC
- K780235 — ORTHOPEDIC DEVICES
- K780231 — BANDAGE, ELASTIC
- K780232 — RESTRAINT, PROTECTIVE
- K780226 — SPREADER BARS
Data sourced from openFDA. This site is unofficial and independent of the FDA.