Smith and Nephew, Inc.
Smith and Nephew, Inc. holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2023.
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.