Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc. - FDA 510(k) C...
Recent clearances: DePuy Synthes Trauma Screws, DePuy Synthes Sterilization Container System, DePuy Synthes Trauma Orthopedic Plates and Screws
5
Total
5
Cleared
0
Denied
Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc. has 5 FDA 510(k) cleared medical devices. Based in 19380, US.
Historical record: 5 cleared submissions from 2017 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc.
5 devices
Cleared
Nov 26, 2019
DePuy Synthes Trauma Screws
Orthopedic
57d
Cleared
May 09, 2019
DePuy Synthes Sterilization Container System
General Hospital
294d
Cleared
Nov 01, 2018
DePuy Synthes Trauma Orthopedic Plates and Screws
Orthopedic
269d
Cleared
Jun 21, 2018
DePuy Synthes (USA) 5.0mm / 7.3mm Crimp Positioning Pins – MR Conditional,...
Orthopedic
267d
Cleared
Jun 30, 2017
DePuy Synthes 4.0 mm and 5.0 mm Locking Screws – MR Conditional, DePuy...
Orthopedic
487d