Symmetry Rapidclean®

RapidClean Grasper; Modular CFH Grasping Forceps; Double-Action; Fenestrated; Ratchet Lock Handle; Slightly Flat Jaws; 5.0 mm; 450 mm

Registry build 21.09.26
46manufacturers in China registered for this device type
75catalogue numbers in this listing
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 Symmetry Rapidclean®
Listed by Aspen Surgical Products, 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, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K974382
Record published 2016-06-13
Record revised 2025-10-29 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date
Sizes Width 5 to 10 mm; length 330 to 450 mm; length 33 to 45 cm; length 13 in
Distribution end date 2022-02-28
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Symmetry Rapidclean®
Catalogue number Size Status
96-1069Q Length 330 mm In distribution
96-1018R Length 330 mm In distribution
96-1051R-45 Length 450 mm In distribution
96-1033Q Length 330 mm In distribution
96-1045Q Length 330 mm In distribution
96-1018Q-45 Length 450 mm In distribution
96-1051Q-45 Length 450 mm In distribution
96-1035Q-45 Length 450 mm In distribution
96-0126-45 Width 10 mm In distribution
96-1008R-45 Length 450 mm In distribution
96-1070R Width 5 mm In distribution
96-1044Q Length 330 mm In distribution
96-1051Q Length 330 mm In distribution
96-1020Q-45 Length 450 mm In distribution
96-1016Q Length 330 mm In distribution
96-1069Q-45 Length 450 mm In distribution
96-2044Q Length 330 mm In distribution
96-1070Q Length 330 mm In distribution
96-1056Q-45 Length 45 cm In distribution
96-1016R Length 330 mm In distribution
96-2020NL-45 Length 45 cm In distribution
96-1022Q Length 330 mm In distribution
96-1035Q Length 330 mm In distribution
96-1033Q-45 Length 450 mm In distribution
96-1063NL Length 330 mm In distribution
96-1042Q-45 Length 450 mm In distribution
96-1030Q-45 Length 450 mm In distribution
96-1056Q Length 330 mm In distribution
96-1035R Length 33 cm In distribution
96-1008Q Length 33 cm In distribution
96-1024R-45 Length 450 mm In distribution
96-1045NL Length 13 in In distribution
96-1050Q Width 5 mm In distribution
96-1050Q-45 Length 450 mm In distribution
96-1030NL-45 Length 450 mm In distribution
96-1009Q Length 33 cm In distribution
96-1072Q Width 10 mm In distribution
96-1042R-45 Length 450 mm In distribution
96-1070Q-45 Length 450 mm In distribution
96-2020Q Length 33 cm In distribution
96-1024Q Width 5 mm In distribution
96-0004TR In distribution
96-1071Q-45 Length 450 mm In distribution
96-1050R-45 Length 450 mm In distribution
96-1015Q-45 Length 450 mm In distribution
96-1018Q Length 330 mm In distribution
96-1063Q Length 330 mm In distribution
96-1044NL Length 330 mm In distribution
96-1015R Length 330 mm In distribution
96-1024Q-45 In distribution
96-2044NL-45 Withdrawn
96-1022NL-45 Withdrawn
96-1018R-45 Withdrawn
96-0126-26 Withdrawn
96-1009Q-45 Withdrawn
96-1016Q-45 Withdrawn
96-1020R-45 Withdrawn
96-1069R-45 Withdrawn
96-1070R-45 Withdrawn
96-1016NL Withdrawn
96-0526-26 Withdrawn
99-11111 Withdrawn
96-1016R-45 Withdrawn
96-1015R-45 Withdrawn
96-1008Q-45 Withdrawn
96-1035R-45 Withdrawn
96-2020Q-45 Withdrawn
96-1056R-26 Withdrawn
96-2044NL Withdrawn
96-1022Q-45 Withdrawn
96-1033NL-45 Withdrawn
96-1056Q-26 Withdrawn
96-1009R-45 Withdrawn
96-1071R-45 Withdrawn
96-1025R 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

Recalls

1 of these is 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
2024-06-03 Class II Process control The affected products may have been packaged with a defect in the sterile barrier seal. As a result, the integrity of the sterile barrier may be compromised. 1900 units
2003-04-30 Not classified Packaging process control Sterility compromised – incomplete sterile package seal. 299 boxes 2003-11-13

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