DePuy Orthopaedics, Inc.
DePuy Orthopaedics, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2026, with 155 FDA device recalls on record.
Clearances by DePuy Orthopaedics, Inc. — page 3
201–208 of 208- K982918 — DEPUY C-STEM SYSTEM
- K982483 — DEPUY MOTECH PEAK FIXATION SYSTEM
- K982011 — DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM
- K981487 — DEPUY GLOBAL SHOULDER GLENOID
- K980595 — DEPUY ORTHOTECH CATERA SUTURE ANCHOR
- K980447 — DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM
- K980513 — ARTICUL/EZE FEMORAL HEADS
- K974044 — GLOBAL TOTAL SHOULDER ECCENTRIC HUMERAL HEAD
Data sourced from openFDA. This site is unofficial and independent of the FDA.