Laparoscope, General & Plastic Surgery

Direct-View Autoclavable Bariatric Laparoscopes 10 MM Outer Diameter, 45 Degree Direction OF View, 81 Degree Field OF View, 330 MM Working Length, Service Replacement

Registry build 21.09.26
46manufacturers in China registered for this device type
118catalogue numbers in this listing
15510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Guangdong (15), Jiangsu (13), Zhejiang (7). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GCJ
Manufacturer City Province Registered as Device types
Hangzhou Kangji Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Hangzhou Endo Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 19
Beilun Plastech Inc Ningbo Zhejiang Contract manufacturer 13
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Qingdao O-MEC Medical Technology Co., Ltd. Qingdao Shandong Contract manufacturer 6
Shenzhen Jingxintai Houseware Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
MediConcepts Technology (Shenzhen) Company Limited Shenzhen Guangdong Contract manufacturer 5
Qisda Electronics (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Barco (Suzhou) Healthcare Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 4
Jiangsu Bana Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 4
Comhuge Medical Wire AND Harness Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 2

Showing 12 of 46. All 46 manufacturers in China registered for Laparoscope, General & Plastic Surgery

Record

Regulatory record for Laparoscope, General & Plastic Surgery
Listed by Smith & Nephew, Inc., United States
FDA product code GCJ
Device type Laparoscope, General & Plastic Surgery
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K980604
Record published 2016-04-12
Record revised 2023-09-07 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Over the counter Yes
Supplied as a kit Yes
Label carries lot or batch number, serial number
Distribution end date 2023-11-07

Catalogue Numbers

Catalogue numbers for Laparoscope, General & Plastic Surgery
Catalogue number Size Status
72202110 In distribution
72202464F In distribution
7210534 In distribution
012606 In distribution
7209340 In distribution
72202465S In distribution
72205161 In distribution
72205164 In distribution
7205609 In distribution
72201919FR In distribution
72205158 In distribution
72205165 In distribution
72202110F In distribution
7209304 In distribution
72200561FR In distribution
72201919 In distribution
4347 In distribution
012603 In distribution
72205168 In distribution
72200561 In distribution
72200599 In distribution
72202464 In distribution
72204926 In distribution
72202111 In distribution
012604 In distribution
012601 In distribution
72205166 In distribution
72202463F In distribution
72201919SR In distribution
72205162 In distribution
72201919F In distribution
72204858 In distribution
72204923 In distribution
012610 In distribution
72202465F In distribution
7205190 In distribution
72205157 In distribution
72202112S In distribution
72202464S In distribution
72203418 In distribution
7206064F In distribution
72204921 In distribution
72203360S In distribution
72205160 In distribution
72202465 In distribution
72202111F In distribution
72205159 In distribution
7207372S In distribution
72205167 In distribution
72202463 In distribution
72203361S In distribution
72205163 In distribution
72200815 In distribution
72200561SR In distribution
72202110S In distribution
72202111S In distribution
7205617D In distribution
72202112 In distribution
72200561S In distribution
72204922 In distribution
72200561F In distribution
72204924 In distribution
7205611 In distribution
012602 In distribution
72202463S In distribution
012605 In distribution
72201919S In distribution
7208333 Withdrawn
7208332 Withdrawn
6900801 Withdrawn
7209361F Withdrawn
7207385F Withdrawn
7210006F Withdrawn
7209340S Withdrawn
2047 Withdrawn
8023S Withdrawn
7207395F Withdrawn
7207946F Withdrawn
7210432S Withdrawn
8015M Withdrawn
7209339 Withdrawn
7210498 Withdrawn
8009S Withdrawn
7207380 Withdrawn
72200593 Withdrawn
72200595 Withdrawn
13525 Withdrawn
7210458F Withdrawn
8018S Withdrawn
7205616 Withdrawn
7210255S Withdrawn
7207951S Withdrawn
6900397 Withdrawn
7210824 Withdrawn
6900398 Withdrawn
72200590 Withdrawn
7208327S Withdrawn
7205193 Withdrawn
7207397S Withdrawn
7205466S Withdrawn
72200596 Withdrawn
7207451 Withdrawn
6900757 Withdrawn
7210345F Withdrawn
72200597 Withdrawn
7209088F Withdrawn
7207375 Withdrawn
72201497 Withdrawn
7206065F Withdrawn
8007Z Withdrawn
7207948F Withdrawn
7209070F Withdrawn
72200042 Withdrawn
7207949S Withdrawn
7210494 Withdrawn
7209290 Withdrawn
2801 Withdrawn
7205193F Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Elmed Elmed, Inc. 3,796
Surgical Direct Surgical Direct, Inc. 2,319
Novo Surgical Novo Surgical, Inc. 1,320
Elmed Incorporated Elmed, Inc. 911
Laparoscope, General & Plastic Surgery Karl Storz GmbH & Co. KG 774
Snowden-Pencer Steris Corporation 693
Millennium Avalign Technologies, Inc. 683
Hermann Medizintechnik GmbH Hermann Medizintechnik Gmbh 615
Clickline Karl Storz GmbH & Co. KG 582
V. Mueller Carefusion 2200, Inc. 553
Grasping forceps Sopro-Comeg GmbH 462
Gimmi Gimmi Gmbh 387

Showing 12 of 1,584. All products under Laparoscope, General & Plastic Surgery

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201198 2020-07-17
K153606 2016-06-02
K070266 2007-02-22
K060777 2006-04-13
K050209 2005-11-23
K032680 2003-09-26
K031379 2003-05-22
K023053 2002-10-03
K011944 2001-09-19
K010489 2001-04-10
K990414 1999-04-14
K980604 1998-05-19
K974592 1998-01-12
K972471 1997-10-24
K971850 1997-08-12

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Laparoscope, General & Plastic Surgery
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Smith & Nephew, Inc. 510(k) number 2011-09-23 Not classified Process design HD1200 camera heads may cause image issues 15 units 2016-02-16

Recalls

The FDA has not published a severity grade for these. 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
2012-03-29 Not classified Nonconforming Material/Component May experience intermittent loss of video
due to a defective board component
239 units 2016-01-13

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