R&D Batteries, Inc.

3.6 Volt .75Ah NiCd (77mm)

Registry build 21.09.26
11manufacturers in China registered for this device type
11catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Beijing (1), Guangdong (1).

Chinese manufacturers registered for FDA product code HLJ
Manufacturer City Province Registered as Device types
Beijing Hongdee Corporation Beijing Beijing Private-label distributor 43
Taizhou City K&W International Trade Co., Ltd. Jiangyan Jiangsu Repacker / relabeller 38
Lianyungang Tiannuo Optical Instrument Co., Ltd. Lianyungang Jiangsu Contract manufacturer 31
66 Vision Tech Co., Ltd. Suzhou Jiangsu Private-label distributor 24
Wuxi Zontai Int’l Corporation Ltd. Wuxi Jiangsu Contract manufacturer 22
Foshan ANY Home Care Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 20
Zumax Medical Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Little Doctor Electronic(Nantong) Co., Ltd. Nantong Jiangsu Contract manufacturer 17
Shanghai Canton Optics Equipment Co., Ltd. Shanghai Shanghai Manufacturer 14
Zhejiang Honsun Medical Technology Co., Ltd. Wenzhou Zhejiang Manufacturer 6
Taihu Huamei Medical Equipment Co., Ltd. Anqing Anhui Contract manufacturer 5

Record

Regulatory record for R&D Batteries, Inc.
Listed by R & D Batteries, Inc., United States
FDA product code HLJ
Device type Ophthalmoscope, Battery-Powered
Device class Class 2
Regulation 21 CFR 886.1570
Establishment Contract manufacturer, Manufacturer
510(k) K942034
Record published 2024-01-01

Specifications

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

Catalogue Numbers

Catalogue numbers for R&D Batteries, Inc.
Catalogue number Size Status
6221 In distribution
6044 In distribution
6220 In distribution
5640 In distribution
6605 In distribution
5224 In distribution
5103 In distribution
6045 In distribution
5124 In distribution
5097 In distribution
5182 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Adstation™ American Diagnostic Corp. 586
Diagnostix™ American Diagnostic Corp. 325
zumax Zumax Medical Co., Ltd. 34
Heine Beta® 200 Diagnostic Set Heine Optotechnik Gmbh & Co. KG. 22
Heine EN 100® Diagnostic Center Heine Optotechnik Gmbh & Co. KG. 20
Welch Allyn, Inc. Welch Allyn, Inc. 17
Heine OMEGA®500 Heine Optotechnik Gmbh & Co. KG. 10
Sunmed SunMed Group Holdings, LLC 6
Heine EN 200® Diagnostic Center Heine Optotechnik Gmbh & Co. KG. 5
Heine K180® Ophthalmoscope Heine Optotechnik Gmbh & Co. KG. 4
Proscope™ American Diagnostic Corp. 4
Eli Ezer U.S. Ophthalmic, L.L.C. 4

Showing 12 of 110. All products under Ophthalmoscope, Battery-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K942034 1994-06-03
K936018 1994-02-22
K936104 1994-02-22

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