Halogen Light Source

Catalogue number OLYMPUS CLK-4, listed by Olympus Medical Systems Corp., Japan, under Forceps, Biopsy, Electric. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (1), Beijing (1), Zhejiang (1).

Chinese manufacturers registered for FDA product code KGE
Manufacturer City Province Registered as Device types
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Beijing Zksk Technology Co., Ltd. Beijing Beijing Contract manufacturer 38
Hangzhou AGS MedTech Co., Ltd. Hangzhou Zhejiang Repacker / relabeller 19

Record

Regulatory record for Halogen Light Source
Listed by Olympus Medical Systems Corp., Japan
FDA product code KGE
Device type Forceps, Biopsy, Electric
Device class Class 2
Regulation 21 CFR 876.4300
Establishment Specification developer, Manufacturer, Exporter
Record published 2016-09-21
Record revised 2024-01-15 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Distribution end date 2024-01-12

Catalogue Numbers

Catalogue numbers for Halogen Light Source
Catalogue number Size Status
OLYMPUS CLK-4 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Forceps, Biopsy, Electric Karl Storz GmbH & Co. KG 32
Zksk Beijing Zksk Technology Co., Ltd. 16
Fujifilm Fujifilm Corporation 15
Fujifilm Diathermic Slitter (FlushKnife) Fujifilm Corporation 13
Forceps, Biopsy, Electric Hangzhou AGS MedTech Co., Ltd. 12
Halyard Avanos Medical, Inc. 9
Single Use Electrosurgical Hemostatic Forceps Olympus Medical Systems Corp. 7
Disposable HOT Biopsy Forceps Olympus Medical Systems Corp. 6
Biopsy Forcep Avanos Medical, Inc. 6
Ensure(TM) Single-Use Coagulation Forceps Micro-Tech (Nanjing) Co., Ltd. 6
ClearHemograsper Finemedix 5
Disposable Hot Biopsy Forceps Micro-Tech (Nanjing) Co., Ltd. 4

Showing 12 of 31. All products under Forceps, Biopsy, Electric

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251807 2026-03-06
K250187 2025-10-07
K171916 2017-10-13
K062517 2006-12-22

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