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Clamp, Surgical, General & Plastic Surgery

FDA product code GDJ · Class 1 · General, Plastic Surgery

2,672
Registered devices
300
Adverse events
9
Recalls
32
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2024-05-16Medtronic Perfusion SystemsIncorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
2024-03-19Medtronic Perfusion SystemsPotential for unsealed sterile packing.
2018-06-29Integra LifeSciences Corp.There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
2018-06-29Integra LifeSciences Corp.There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
2018-06-29Integra LifeSciences Corp.There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
2018-06-29Integra LifeSciences Corp.There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
2013-07-02Stryker Howmedica Osteonics Corp.Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
2005-04-06Smith & Nephew, Inc., Endoscopy Div.Cupped Grasper Handle marked incorrectly as Duckbill Upbiter

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.