Smith and Nephew, Inc.
FDA 510(k) medical device clearances.
Top product codes for Smith and Nephew, Inc.
Recent clearances by Smith and Nephew, Inc.
- K222501 — Regeneten Bioinductive Implant
- K221740 — SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NETWORK ENABLED (72205447), SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NON-NETWORK ENABLED (72205448)
- K191177 — LENS 4K Camera Control Unit - Wifi, LENS 4K Camera Control Unit - Non-Wifi, LENS 4K Camera Head
- K183232 — Double ENDOBUTTON Fixation Device
- K181746 — MICRORAPTOR Knotless Suture Anchor
- K180361 — MICRORAPTOR REGENESORB Suture Anchor
- K163034 — SUTUREFIX Curved Suture Anchor
Data sourced from openFDA. This site is unofficial and independent of the FDA.