Smith and Nephew, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smith and Nephew, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Regeneten Bioinductive Implant, SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NETWORK ENABLED (72205447), SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NON-NETWORK ENABLED (72205448), LENS 4K Camera Control Unit - Wifi, LENS 4K Camera Control Unit - Non-Wifi, LENS 4K Camera Head
7
Total
7
Cleared
0
Denied
Smith and Nephew, Inc. has 7 FDA 510(k) cleared medical devices. Based in Andover, US.
Last cleared in 2023. Active since 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Smith and Nephew, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Smith and Nephew, Inc.
7 devices
Cleared
May 11, 2023
Regeneten Bioinductive Implant
Orthopedic
266d
Cleared
Oct 20, 2022
SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NETWORK ENABLED (72205447),...
General & Plastic Surgery
127d
Cleared
Aug 23, 2019
LENS 4K Camera Control Unit - Wifi, LENS 4K Camera Control Unit - Non-Wifi,...
General & Plastic Surgery
113d
Cleared
Mar 12, 2019
Double ENDOBUTTON Fixation Device
Orthopedic
112d
Cleared
Sep 28, 2018
MICRORAPTOR Knotless Suture Anchor
Orthopedic
88d
Cleared
May 30, 2018
MICRORAPTOR REGENESORB Suture Anchor
Orthopedic
110d
Cleared
Dec 07, 2016
SUTUREFIX Curved Suture Anchor
Orthopedic
37d