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Clip, Implantable

FDA product code FZP · Class 2 · General, Plastic Surgery

1,257
Registered devices
42,203
Adverse events
45
Recalls
177
510(k) clearances

Devices with this code

Mammotome MAMMOMARK 2 — DEVICOR MEDICAL PRODUCTS, INC.WECK — TELEFLEX INCORPORATEDPAD/CHAM — APPLIED MEDICAL RESOURCES CORPORATIONUltraClip® II Breast Tissue Marker — Bard Peripheral Vascular, Inc.CNGL3 - ALBRECHT — APPLIED MEDICAL RESOURCES CORPORATIONWECK — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDLAP CHOLE KIT - DR. BOYER — APPLIED MEDICAL RESOURCES CORPORATIONCHOLE KIT 1 — APPLIED MEDICAL RESOURCES CORPORATIONDR. WARE — APPLIED MEDICAL RESOURCES CORPORATIONLAP CHOLE KIT — APPLIED MEDICAL RESOURCES CORPORATIONE-PACK — Ethicon Inc.WECK — TELEFLEX INCORPORATEDE-PACK — Ethicon Inc.WECK — TELEFLEX INCORPORATEDSLS-CLIP — VITALITEC SURGICALWECK — TELEFLEX INCORPORATEDTELEFLEX — TELEFLEX INCORPORATEDWECK — TELEFLEX INCORPORATEDREFLECTION, MICROSTABLE — Smith & Nephew, Inc.KIT LAP CHOL MCA — APPLIED MEDICAL RESOURCES CORPORATIONTOTAL 5mm SOLUTION KIT — APPLIED MEDICAL RESOURCES CORPORATIONKIT KE177 COLE HASSON — APPLIED MEDICAL RESOURCES CORPORATIONSINGLE SITE LAP CHOLE KIT — APPLIED MEDICAL RESOURCES CORPORATION

Recent recalls

DateFirmReason
2023-04-28TELEFLEX LLCTeleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts t
2021-04-16Aesculap Implant Systems LLCMalfuncton-Implant did not deploy successfully may necessitate the need for an additional medical intervention for patients which would result in a potential de
2021-04-16Aesculap Implant Systems LLCMalfuncton-Implant did not deploy successfully may necessitate the need for an additional medical intervention for patients which would result in a potential de
2020-09-17Genicon, Inc.Device malfunction causing the applier to jam, and clip loading failures.
2019-11-07Ethicon Endo-Surgery IncA potential exists that certain LIGAMAX devices within the impacted lots may have small holes in the Tyvek lidding which could result in a breach of sterility.
2019-10-04Teleflex MedicalCertain clip appliers have an increase in misloading and/or jamming related complaints that may be due to a discrepancy in the specification a component. Misloa
2019-10-04Teleflex MedicalCertain clip appliers have an increase in misloading and/or jamming related complaints that may be due to a discrepancy in the specification a component. Misloa
2018-04-02AESDEXFollowing pressurization of the devices, damage to the device handle mechanism may occur, accompanied by a loud noise and potential dispersion of plastic fragme
2018-04-02AESDEXFollowing pressurization of the devices, damage to the device handle mechanism may occur, accompanied by a loud noise and potential dispersion of plastic fragme
2018-01-22Aesculap Implant Systems LLCAdded a contraindication to IFU: Do not use the DS clips for living donor nephrectomies. Added other contraindications. A publication from 2017 recommended Aes

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