Signature

Locking Long Single Action Retraction Grasping Forceps

Registry build 21.09.26
65manufacturers in China registered for this device type
91catalogue numbers in this listing
8recalls on this code

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 Signature
Listed by Silex Medical, LLC, United States
FDA product code GEI
Device type Electrosurgical, Cutting & Coagulation & Accessories
Device class Class 2
Regulation 21 CFR 878.4400
Establishment Manufacturer
510(k) K914910
Record published 2018-02-13
Record revised 2019-08-21 (version 4)

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, serial number

Catalogue Numbers

Catalogue numbers for Signature
Catalogue number Size Status
5864110 In distribution
5851045 In distribution
5863020 In distribution
5851051 In distribution
5864110-45 In distribution
5881063 In distribution
5851064-45 In distribution
5851089 In distribution
5861020 In distribution
5881024 In distribution
5881018 In distribution
5851087 In distribution
5881005 In distribution
5851087-45 In distribution
5862030 In distribution
5851050 In distribution
5851034 In distribution
5851004 In distribution
5851079 In distribution
5851034-45 In distribution
5851033 In distribution
5881007 In distribution
5862080-45 In distribution
5862080 In distribution
5862000-45 In distribution
5851044-45 In distribution
5851067-45 In distribution
5881056-45 In distribution
5851071-45 In distribution
5861020-45 In distribution
5851069-45 In distribution
5851069 In distribution
5862100-45 In distribution
5881068 In distribution
5851088-45 In distribution
5861000-45 In distribution
5881018-45 In distribution
5862100 In distribution
5862080 In distribution
5851035-45 In distribution
5881056 In distribution
5860030-45 In distribution
5881005-45 In distribution
5851066 In distribution
5851052 In distribution
5863050 In distribution
5860020 In distribution
5851037 In distribution
5851088 In distribution
5851078 In distribution
5863000-45 In distribution
5851035 In distribution
5863020 In distribution
5881012-45 In distribution
5851091-45 In distribution
5851075-45 In distribution
5872130 In distribution
5851045-45 In distribution
5851093 In distribution
5851092-45 In distribution
5851066-45 In distribution
5851092 In distribution
5851064 In distribution
5851051-45 In distribution
5851044 In distribution
5851053-45 In distribution
5851037 In distribution
5851050-45 In distribution
5860020-45 In distribution
5881024-45 In distribution
5851037-45 In distribution
5851093-45 In distribution
5851052-45 In distribution
5862110 In distribution
5881063-45 In distribution
5851002 In distribution
5851067 In distribution
5862100 In distribution
5851072-45 In distribution
5851078-45 In distribution
5881030 In distribution
5863020-45 In distribution
5851053 In distribution
5881003 In distribution
5860040 In distribution
5851002-45 In distribution
5851032-45 In distribution
5851072 In distribution
5864110 In distribution
5851033-45 In distribution
5851032 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

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

Recalls naming the identifiers of Signature
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 2 units
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 10 units
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 8 units
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 29 units
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 6 units
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 7 units
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 105 units
Silex Medical, LLC 510(k) number 2024-01-09 Class II Process control Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel. 2 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