Welch Allyn, Inc.

Welch Allyn Green Series 777 Integrated Wall Diagnostic System including Wall Aneroid Sphygmomanometer (#7670-01), SureTemp Plus 690 Electronic Thermometer (#01690-300), Coaxial…

Registry build 21.09.26

Welch Allyn Green Series 777 Integrated Wall Diagnostic System including Wall Aneroid Sphygmomanometer (#7670-01), SureTemp Plus 690 Electronic Thermometer (#01690-300), Coaxial Ophthalmoscope (#11720), MacroView Otoscope (#23810), SureColor LED Lamp Technology, KleenSpec Disposable Specula Dispenser, Wall-Mount Panel (34 x 12 in / 86.4 x 30.5 cm)

70manufacturers in China registered for this device type
66catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (46), Jiangsu (7), Beijing (5). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQA
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Tianjin Choice Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 12
Taijia Medical Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
EMI (Dongguan) Asia Limited Dongguan Guangdong Contract manufacturer 9
Wuhan Strong Electronics Wuhan Hubei Contract manufacturer 6
Regent Electron Suzhou Co., Ltd. Wujiang Jiangsu Contract manufacturer 5
Dongguan Ruibaolian Medical Science & Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Dongguan Kepler Special Cabling Company Limited Dongguan Guangdong Contract manufacturer 3
Measurement Specialties Chengdu Chengdu Sichuan Contract manufacturer 3
Beijing Kingst Commercial & Trade Co., Ltd. Beijing Beijing Contract manufacturer 2
Suzhou Meccan Import and Export Corp. Suzhou Jiangsu Contract manufacturer 71
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61

Showing 12 of 70. All 70 manufacturers in China registered for Oximeter

Record

Regulatory record for Welch Allyn, Inc.
Listed by Welch Allyn, Inc., United States
FDA product code DQA
Device type Oximeter
Device class Class 2
Regulation 21 CFR 870.2700
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K101680
Record published 2017-12-05
Record revised 2025-08-11 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Prescription Prescription only
Over the counter Yes
Label carries lot or batch number, manufacturing date, serial number
Distribution end date 2026-03-06

Catalogue Numbers

Catalogue numbers for Welch Allyn, Inc.
Catalogue number Size Status
901012 In distribution
901055 In distribution
901065 In distribution
901057 In distribution
901055 In distribution
901057 In distribution
901057 In distribution
901055 In distribution
901055 In distribution
901056 In distribution
901027 In distribution
901057 In distribution
901113 In distribution
901056 In distribution
901057 In distribution
901055 In distribution
901057 In distribution
901113 In distribution
901012 In distribution
901057 In distribution
901057 In distribution
901055 In distribution
901055 In distribution
901055 In distribution
901057 In distribution
901055 In distribution
901055 In distribution
901012 In distribution
901055 In distribution
901057 In distribution
901055 In distribution
901057 In distribution
901057 In distribution
901055 In distribution
901012 In distribution
901057 In distribution
901012 In distribution
901057 In distribution
901055 In distribution
901011 In distribution
901055 In distribution
901056 Withdrawn
901012 Withdrawn
901056 Withdrawn
901056 Withdrawn
901056 Withdrawn
901011 Withdrawn
901056 Withdrawn
901056 Withdrawn
901057 Withdrawn
901057 Withdrawn
901010 Withdrawn
901056 Withdrawn
901056 Withdrawn
901056 Withdrawn
901056 Withdrawn
901065 Withdrawn
901056 Withdrawn
901056 Withdrawn
901012 Withdrawn
901056 Withdrawn
901000 Withdrawn
901056 Withdrawn
901055 Withdrawn
901056 Withdrawn
901056 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Unimed Unimed Medical Supplies Inc 2,838
APK APK Technology Co., Ltd. 2,678
ChoiceMMed Beijing Choice Electronic Technology Co., Ltd. 151
Nellcor Covidien LP 138
Nonin Nonin Medical, Inc. 129
Orantech Orantech Inc. 97
Med-link Shenzhen MED-Link Electronics Tech Co., Ltd. 93
Medichoice Owens & Minor Distribution, Inc. 62
Caremed Shenzhen Caremed Medical Technology Co., Ltd. 55
Sensoronics Sensoronics Incorporated 53
Virtuox Healthcare Logistics Systems 36
AMC LifeSync Corporation 36

Showing 12 of 1,063. All products under Oximeter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K053381 2006-06-15
K022084 2002-09-26
K022163 2002-09-17

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