Ligaclip

Ligaclip Clip Applier Medium-Large, Angled Jaw, 26.7cm

Registry build 21.09.26
9manufacturers in China registered for this device type
29catalogue numbers in this listing
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Zhejiang (2), Shandong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GDO
Manufacturer City Province Registered as Device types
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Jiangsu Bana Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 4
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Bothwin (Beijing) Medical Technology Co., Ltd. Beijng Beijing Manufacturer 25
Tonglu Wanhe Medical Instrument Co., Ltd. Hangzhou Zhejiang Manufacturer 24
Hangzhou Tonglu Shikonghou Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 17
Tianjin Huahong Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 6
Sinolinks Medical Innovation, Inc. Changzhou Jiangsu Complaint-file establishment 5
Fengh Medical Co., Ltd. Jiangyin Jiangsu Manufacturer 4

Record

Regulatory record for Ligaclip
Listed by Ethicon Endo-Surgery, Inc., United States
FDA product code GDO
Device type Applier, Surgical, Clip
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Specification developer, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-07-15
Record revised 2023-07-31 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide, Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Case of 25, case of 100, case of 50, case of 24, box of 6, case of 5

Catalogue Numbers

Catalogue numbers for Ligaclip
Catalogue number Size Status
LC800 In distribution
MCM30 In distribution
LX320 In distribution
LX105 In distribution
LX307 In distribution
LX220 In distribution
LX430 In distribution
LC420 In distribution
LC307 In distribution
LX205 In distribution
LX230 In distribution
LX130 In distribution
LX310 In distribution
LX110 In distribution
LX107 In distribution
LC430 In distribution
MSM20 In distribution
LX210 In distribution
LC410 In distribution
MCS20 In distribution
MCL20 In distribution
LX420 In distribution
LC407 In distribution
LC320 In distribution
LX407 In distribution
LC310 In distribution
LX207 In distribution
MCM20 In distribution
LX410 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Weck Teleflex Medical LLC 996
Teleflex Teleflex Medical LLC 61
Aesculap Aesculap AG 46
Surgical Direct Surgical Direct, Inc. 28
Elmed Elmed, Inc. 23
RZ Medizintechnik GmbH RZ Medizintechnik Gmbh 19
Ambler Surgical Ambler Surgical, LLC 19
Europclip Ackermann Instrumente Gmbh 17
Lazic Peter Lazic Gmbh 15
Artisential Clip Applier Large LivsMed Inc. 14
Artisential Clip Applier Medium Large LivsMed Inc. 14
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 11

Showing 12 of 73. All products under Applier, Surgical, Clip

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2013-04-12 Class II Under Investigation by firm Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP 10mm M/L Endoscopic Rotating Multiple Clip Applier (ER320) due to potential clip formation and feeding issues which may result in improper clip formation, vessel damage and/ 738,356 2014-05-01
2013-04-12 Class II Under Investigation by firm Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP 10mm M/L Endoscopic Rotating Multiple Clip Applier (ER320) due to potential clip formation and feeding issues which may result in improper clip formation, vessel damage and/ 49,357 2014-05-01
2013-04-12 Class II Under Investigation by firm Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP 10mm M/L Endoscopic Rotating Multiple Clip Applier (ER320) due to potential clip formation and feeding issues which may result in improper clip formation, vessel damage and/ 10,488 2014-05-01
2004-06-07 Not classified Other This device is subject to recall due to an increased possibility of clip scissoring which can result in less than optimal clip formation which may or may not securely ligate tubular structures. 120,4015 2008-10-29

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer