Medline

CLAMP,CIRCUMCISION,1.3CM,NONSTERILE

Registry build 21.09.26
2manufacturers in China registered for this device type
3catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (1), Anhui (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HFX
Manufacturer City Province Registered as Device types
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
Wuhu Snnda Medical Treatment Appliance Technology Co., Ltd. Wuhu Anhui Manufacturer 1

Record

Regulatory record for Medline
Listed by Medline Industries, Inc., United States
FDA product code HFX
Device type Clamp, Circumcision
Device class Class 2
Regulation 21 CFR 884.4530
510(k) K212911
Record published 2026-01-12
Record revised 2026-06-15 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number
Distribution end date 2022-08-27
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Medline
Catalogue number Size Status
MDS9900025K In distribution
MDS10781 In distribution
MDS10780 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ShangRing Wuhu Snnda Medical Treatment Appliance Technology Co., Ltd. 24
Centurion Centurion Medical Products Corporation 18
Devon Cardinal Health 17
Gomco Circumcision Clamp Sontec Instruments, Inc. 16
Gomco Allied Medical LLC 9
Circumplast Emboss Medical Limited 8
Aesculap Aesculap AG 6
Medical Action Industries Medical Action Industries, Inc. 4
AccuCirc® Clinical Innovations, LLC 4
Gomco Type Circumcision Clamp Fine Surgical Instruments Inc. 4
Mogen Circumcision Clamp Sontec Instruments, Inc. 2
Gomco Circumcision Clamp Chrome Sontec Instruments, Inc. 2

Showing 12 of 21. All products under Clamp, Circumcision

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K212911 2022-11-18

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