Smith & Nephew Inc., Endoscopy Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smith & Nephew Inc., Endoscopy Div. - FDA 510(k) Cleared Devices
Recent clearances: REGENETEN™ Bioinductive Implant
10
Total
10
Cleared
0
Denied
Smith & Nephew Inc., Endoscopy Div. has 10 FDA 510(k) cleared orthopedic devices. Based in Andover, US.
Latest FDA clearance: Nov 2024. Active since 2007.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Smith & Nephew Inc., Endoscopy Div.
10 devices
Cleared
Nov 26, 2024
REGENETEN™ Bioinductive Implant
Orthopedic
84d
Cleared
Nov 14, 2011
ACUFEX DIRECTOR APPLICATION ANATOMIC GUIDE SYSTEM
Orthopedic
138d
Cleared
Jan 05, 2011
SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY
General Hospital
124d
Cleared
Sep 14, 2010
SMITH & NEPHEW INSTRUMENT TRAYS
General Hospital
390d
Cleared
Apr 19, 2010
SMITH AND NEPHEW TWINFIX ULTRA TI SUTURE ANCHOR
Orthopedic
89d
Cleared
Mar 05, 2010
BIOSURE SYNC TIBIAL FIXATION DEVICE, 6MM, 8MM,10MM,12MM
Orthopedic
73d
Cleared
Mar 04, 2010
SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR
Orthopedic
76d
Cleared
May 21, 2008
SMITH & NEPHEW INSTRUMENT TRAYS
General Hospital
155d
Cleared
Apr 23, 2008
PLLA, HA SCREW
Orthopedic
72d
Cleared
Mar 06, 2007
PLC SUTURE ANCHOR
Orthopedic
81d