ClearHemograsper

The FDA filing identifies ClearHemograsper as an endoscopic hemostasis forceps. It describes a monopolar instrument used with an endoscope in the digestive tract. The filing says it uses…

Registry build 21.09.26

The FDA filing identifies ClearHemograsper as an endoscopic hemostasis forceps. It describes a monopolar instrument used with an endoscope in the digestive tract.

The filing says it uses high-frequency current to coagulate or perform hemostasis. It may assist in endoscopic procedures such as endoscopic submucosal dissection.

Listed Item

5mm/ 1,820mm/ Dial

Components and Operation

The device has a slider, catheter tube, pair of jaws, plug and irrigation port. The jaws catch the bleeding site and deliver current; the port injects distilled water or saline to remove foreign substances.

3manufacturers in China registered for this device type
5catalogue numbers in this listing
1510(k) clearance

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 ClearHemograsper
Listed by Finemedix, South Korea
FDA product code KGE
Device type Forceps, Biopsy, Electric
Device class Class 2
Regulation 21 CFR 876.4300
Establishment Manufacturer
510(k) K242857
Record published 2026-03-24

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Box of 5

Catalogue Numbers

Catalogue numbers for ClearHemograsper
Catalogue number Size Status
FM-HG0001(1820) In distribution
FM-HG0001(1820)B In distribution
FM-HG0001(2000) In distribution
FM-HG0001(1650) In distribution
FM-HG0001(2300)B In distribution

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
Disposable Hot Biopsy Forceps Micro-Tech (Nanjing) Co., Ltd. 4
Precisor ConMed Corporation 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
K242857 2025-05-21

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