Walcott Rx

Reusable Bipolar Forceps 4" (10.2cm) Jewelers, Straight 0.4mm Tips

Registry build 21.09.26
65manufacturers in China registered for this device type
22catalogue numbers in this listing

Who Else Makes It

Concentrated in Guangdong (24), Zhejiang (13), Shanghai (10). 23 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GEI
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Hangzhou Kangji Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Hangzhou Endo Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 19
Hong Qiangxing (Shen Zhen) Electronics Limited Shenzhen Guangdong Contract manufacturer 19
Shenzhen MED-Link Electronics Tech Co., Ltd. Shenzhen Guangdong Contract manufacturer 18
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Jiangyin Sinbon Electronics Co Ltd Jiangyin Jiangsu Contract manufacturer 13
Guangzhou Huada Biotechnology Co., Ltd. Guangzhou Guangdong Contract manufacturer 9

Showing 12 of 65. All 65 manufacturers in China registered for Electrosurgical, Cutting & Coagulation & Accessories

Record

Regulatory record for Walcott Rx
Listed by Walcott Rx Product Inc
FDA product code GEI
Device type Electrosurgical, Cutting & Coagulation & Accessories
Device class Class 2
Regulation 21 CFR 878.4400
510(k) K864402
Record published 2016-07-04
Record revised 2022-07-11 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Radiation Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack of 50, pack of 10, pack of 25, pack of 5
Sizes Length 10 to 12 ft; length 3.5 to 4 in

Catalogue Numbers

Catalogue numbers for Walcott Rx
Catalogue number Size Status
RX14-5009 In distribution
RX14-7002 In distribution
RX14-5011 In distribution
RX10-3000 Length 4 in In distribution
RX14-5004 In distribution
RX14-3000 Length 4 in In distribution
RX12-1075 Length 3.5 in In distribution
RX14-5002 In distribution
RX14-7006 In distribution
RX12-1080 Length 3.5 in In distribution
RX10-6075 Length 12 ft In distribution
RX10-5000 Length 12 ft In distribution
RX10-4000 Length 12 ft In distribution
RX14-7009 In distribution
RX10-6000 Length 12 ft In distribution
RX14-5007 In distribution
RX14-5006 In distribution
RX30-1203 Length 10 ft In distribution
RX14-7000 In distribution
RX14-7008 In distribution
RX10-6060 Length 12 ft In distribution
RX14-5000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Surgical Direct Surgical Direct, Inc. 5,729
Speedlock National Advanced Endoscopy Devices, Inc. 5,212
Stingray Surgical Products Stingray Surgical Products L.L.C. 4,647
Kirwan Kirwan Surgical Products, LLC. 1,901
Millennium Avalign Technologies, Inc. 1,779
DANmed Dannoritzer Medizintechnik GmbH & Co. KG 1,590
Elmed Elmed, Inc. 1,519
Symmetry Olsen Aspen Surgical Products, Inc. 1,219
Guenter Bissinger Medizintechnik GmbH Günter Bissinger Medizintechnik GmbH 1,117
Ambler Surgical Ambler Surgical, LLC 756
V. Mueller Steris Corporation 661
Aesculap Aesculap AG 544

Showing 12 of 2,922. All products under Electrosurgical, Cutting & Coagulation & Accessories

Recalls Naming This Product

7 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Walcott Rx
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Kirwan Surgical Products, LLC. 510(k) number 2024-11-14 Class I Device Design Potential for the outer stainless-steel tube to break or detach. 80,060 units
Kirwan Surgical Products, LLC. 510(k) number 2024-11-14 Class I Device Design Potential for the outer stainless-steel tube to break or detach. 66 units
Kirwan Surgical Products, LLC. 510(k) number 2024-11-14 Class I Device Design Potential for the outer stainless-steel tube to break or detach. 800 units
Kirwan Surgical Products, LLC. 510(k) number 2024-11-14 Class I Device Design Potential for the outer stainless-steel tube to break or detach. 4,470 units
Kirwan Surgical Products, LLC. 510(k) number 2024-11-14 Class I Device Design Potential for the outer stainless-steel tube to break or detach. 3,010 units
Kirwan Surgical Products, LLC. 510(k) number 2024-11-14 Class I Device Design Potential for the outer stainless-steel tube to break or detach. 925 units
Kirwan Surgical Products, LLC. 510(k) number 2024-11-14 Class I Device Design Potential for the outer stainless-steel tube to break or detach. 2,999 units

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