Medical Device Manufacturer · US , Andover , MA

Smith and Nephew, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2016

7

Total

7

Cleared

0

Denied

Smith and Nephew, Inc. has 7 FDA 510(k) cleared medical devices. Based in Andover, US.

Latest FDA clearance: May 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.

7 devices

1–7 of 7

Regeneten Bioinductive Implant

K222501 · OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon · Orthopedic

SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NETWORK ENABLED (72205447), SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NON-NETWORK ENABLED (72205448)

K221740 · GCJ Laparoscope, General & Plastic Surgery · General & Plastic Surgery

LENS 4K Camera Control Unit - Wifi, LENS 4K Camera Control Unit - Non-Wifi, LENS 4K Camera Head

K191177 · GCJ Laparoscope, General & Plastic Surgery · General & Plastic Surgery

Double ENDOBUTTON Fixation Device

K183232 · HTN Washer, Bolt Nut · Orthopedic

MICRORAPTOR Knotless Suture Anchor

K181746 · MAI Fastener, Fixation, Biodegradable, Soft Tissue · Orthopedic

MICRORAPTOR REGENESORB Suture Anchor

K180361 · MAI Fastener, Fixation, Biodegradable, Soft Tissue · Orthopedic

SUTUREFIX Curved Suture Anchor

K163034 · MBI Fastener, Fixation, Nondegradable, Soft Tissue · Orthopedic