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Smith and Nephew, Inc.

7 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Regeneten Bioinductive Implant (K222501)Smith and Nephew, Inc.2023-05-11
SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NETWORK ENABLED (72205447), SMITH & NEPHEW INTELLIO 4K CAMERA CONTROL UNIT, NON-NETWORK ENABLED (72205448) (K221740)Smith and Nephew, Inc.2022-10-20
LENS 4K Camera Control Unit - Wifi, LENS 4K Camera Control Unit - Non-Wifi, LENS 4K Camera Head (K191177)Smith and Nephew, Inc.2019-08-23
Double ENDOBUTTON Fixation Device (K183232)Smith and Nephew, Inc.2019-03-12
MICRORAPTOR Knotless Suture Anchor (K181746)Smith and Nephew, Inc.2018-09-28
MICRORAPTOR REGENESORB Suture Anchor (K180361)Smith and Nephew, Inc.2018-05-30
SUTUREFIX Curved Suture Anchor (K163034)Smith and Nephew, Inc.2016-12-07

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Every clearance here is in the API, with alerts when new ones post.