Welch Allyn, Inc.

GS Series Mobile Stand

Registry build 21.09.26
18manufacturers in China registered for this device type
3catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Guangdong (5), Shanghai (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KZF
Manufacturer City Province Registered as Device types
Ningbo Hongbo Optical Instrument Co., Ltd. Ningbo Zhejiang Contract manufacturer 1
Shanghai MU Promotions Co., Ltd. Shanghai Shanghai Exporter 62
Orantech Inc. Shenzhen Guangdong Contract manufacturer 40
Danyang NEW Hope Medical Equipment Co., Ltd. Danyang Jiangsu Manufacturer 38
Hebei Ruinuo Medical Instrument Co Ltd Shijiazhuang Hebei Manufacturer 29
Jiangsu Keling Medical Appliances Co., Ltd. Yangzhou Jiangsu Contract manufacturer 23
Zumax Medical Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Jiangsu Liangxu Intelligence Science AND Technology Co., Ltd. Nanjing Jiangsu Contract manufacturer 12
Zhongshan Meiyigou Electronics Co., Ltd. Zhongshan Guangdong Manufacturer 11
Alltion (Guangxi) Instrument Co., Ltd. Wuzhou Guangxi Manufacturer 8
Nanchang Micare Medical Equipment Co., Ltd. Nanchang Jiangxi Manufacturer 8
Shanghai PAX Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 7

Showing 12 of 18. All 18 manufacturers in China registered for Device, Medical Examination, Ac Powered

Record

Regulatory record for Welch Allyn, Inc.
Listed by Welch Allyn, Inc., United States
FDA product code KZF
Device type Device, Medical Examination, Ac Powered
Device class Class 1
Regulation 21 CFR 880.6320
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2024-08-14
Record revised 2024-12-11 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Over the counter Yes
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Welch Allyn, Inc.
Catalogue number Size Status
901189 In distribution
901189 In distribution
901189 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Celestial Star Sunnex, Inc. 27
ACEMST1 Acem SPA 22
HexaLux Steris Corporation 18
Vista LED Avante 16
MI Product Line Medical Illumination International, Inc 16
Tri Star Sunnex, Inc. 14
Verilux Bear Down Consulting 14
Midmark Midmark Corporation 14
Ritter Midmark Corporation 13
PF Sunnex, Inc. 13
Kenex Kenex (Electro-Medical) Ltd. 13
Lucea LED® Maquet Gmbh 12

Showing 12 of 63. All products under Device, Medical Examination, Ac Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K952835 1995-09-22
K934259 1994-01-28
K921493 1992-11-03
K920103 1992-04-28
K852949 1985-09-04
K780628 1978-06-06

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