Weck Hem-o-lok Auto Endo5 Ligating Clip Applier

FDA 510(k) K142777 · Teleflexmedical, Inc.

Substantially Equivalent

510(k) numberK142777

Submission

Device name
Weck Hem-o-lok Auto Endo5 Ligating Clip Applier
Applicant
Teleflexmedical, Inc.
Durham, NC, US
Received
September 26, 2014
Decision date
December 19, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FZP – Clip, Implantable
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4300
Specialty
General, Plastic Surgery
Implant
Yes

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K254231Inno-Hook™ Disposable Clip Appliers (Ligating Clips) and Inno-Hook™ Ligating ClipsFZP · Traditional Taiwan Surgical Corporation07/20/2026SE
K253903InnoClip Disposable Clip ApplierFZP · Special Taiwan Surgical Corporation12/22/2025SE
K253781InnoClip Clip ApplierFZP · Special Taiwan Surgical Corporation12/22/2025SE
K250643Disposable Polymer Ligation ClipsFZP · Traditional Hangzhou Kangji Medical Instrument Co., Ltd.11/20/2025SE
K251054Hem-o-lok™ PurplePlus™ Large Polymer Ligating ClipsFZP · Traditional Teleflex Medical07/03/2025SE
K242541Gem ZipclipFZP · Traditional Synovis Micro Companies Alliance A Subsidiary of…01/15/2025SE
K221495SOLID CLIP™ Single Use Clip ApplierFZP · Traditional Medscope Biotech Co., Ltd.07/18/2024SE
K232970Hem-o-lok® Ligating ClipsFZP · Traditional Teleflex Medical01/12/2024SE
K230966angiOCCLUDE Ligating ClipsFZP · Traditional A2 Medical Systems, LLC09/19/2023SE
K232313LIGACLIP Endoscopic Rotating Multiple Clip Applier 12mm L (ER420); LIGACLIP Endoscopic…FZP · Special Ethicon Endo Surgery, LLC08/29/2023SE

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Questions and answers

When was Weck Hem-o-lok Auto Endo5 Ligating Clip Applier cleared by the FDA?

Weck Hem-o-lok Auto Endo5 Ligating Clip Applier (K142777) received a 510(k) decision of Substantially Equivalent on December 19, 2014, 84 days after the submission was received.

What is the product code of K142777?

The FDA product code is FZP – Clip, Implantable, a Class II (moderate risk) device regulated under 21 CFR 878.4300.