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Laparoscopic Contraceptive Tubal Occlusion Device

FDA product code KNH · Class 3 · Obstetrics/Gynecology

32
Registered devices
892
Adverse events
4
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-10-21Gyrus Acmi, IncorporatedAll packages of Falope Ring Band Applicator kits are being recalled due to compromises in sterile packaging that could be associated with bacterial contaminatio
2014-07-09Richard Wolf Medical Instruments Corp.Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal Occluding Device lot 51000232. The devices are being recalled as a part of an investig
2014-07-08Gyrus Medical, IncFalope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold as a stand-alone non-sterile component. The dilator is intended to assist placemen
2014-02-19Gyrus Medical, IncDue to an anomaly in the packaging process for specific lots of Disposable Falope-Ring Band Kit, it is possible that a defective seal could be present that may

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