Medline

SPONGE,LAP,18"X18",STD,XR,ST,5/PK,40PK/C

Registry build 21.09.26
67manufacturers in China registered for this device type
41catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (18), Hubei (13), Zhejiang (12). 17 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GDY
Manufacturer City Province Registered as Device types
Shanghai Joy Crown Industry Co., Ltd. Pu Dong New Area Shanghai Contract manufacturer 64
Allmed Medical Products Co., Ltd. Zhijiang Hubei Contract manufacturer 43
BH Medical Products Co., Ltd. Changzhou Jiangsu Contract manufacturer 37
Jiangsu JianYu Health Medical Co., Ltd. Changzhou Jiangsu Contract manufacturer 35
Jiangsu Guangda Medical Material Group Co., Ltd. Haian Jiangsu Contract manufacturer 32
Jingmen Huasheng Asia Dynamics Sanitary Products Co., Ltd. Jingmen Hubei Contract manufacturer 23
Derma Sciences Nantong Incorporation Development Jiangsu Contract manufacturer 19
Kingstar Medical (Xianning) Co., Ltd. Xianning Hubei Contract manufacturer 17
Zhejiang Aoki Medical Dressing Co., Ltd. Wenzhou Zhejiang Contract manufacturer 16
Qingdao Likangyuan Medical Device Co., Ltd. Qingdao Shandong Contract manufacturer 14
Winner Medical (Chongyang) Co., Ltd. Chongyang Hubei Contract manufacturer 13
Suzhou Avon Textile Co., Ltd. Suzhou Jiangsu Contract manufacturer 12

Showing 12 of 67. All 67 manufacturers in China registered for Gauze/Sponge, Internal, X-Ray Detectable

Record

Regulatory record for Medline
Listed by Medline Industries, Inc., United States
FDA product code GDY
Device type Gauze/Sponge, Internal, X-Ray Detectable
Device class Class 1
Regulation 21 CFR 878.4450
Premarket notification Exempt
Record published 2021-03-22
Record revised 2025-05-23 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Over the counter Yes
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Keep Dry, Keep away from sinlight
Packaging Case of 20, case of 40, case of 200, case of 100
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Medline
Catalogue number Size Per pack Status
MDS251512LF In distribution
MDS251518DLX In distribution
MDS251518LFT 10 In distribution
MDS241518XI 5 In distribution
BNS32679 200 In distribution
MDS253636LF In distribution
NON21438 10 In distribution
NON21432LF 10 In distribution
NON216645 In distribution
BNS119382 200 In distribution
NON25856 2 In distribution
MDS251518NLLF 5 In distribution
MDS50403 In distribution
MDS241518T In distribution
NON21433 10 In distribution
MDS251518LF 5 In distribution
MDS251518RNG 5 In distribution
DNSCTM05230 In distribution
BNS119376 5 In distribution
MDS251512RLF In distribution
BNS83465 200 In distribution
MDS251726LF 5 In distribution
MDS74712 5 In distribution
MDS241518 5 In distribution
NON21430LF 10 In distribution
NON21425 In distribution
MDS231318LF 5 In distribution
BNS119384 200 In distribution
MDS251836LF5 5 In distribution
NON21430LFPP 10 In distribution
NON21432CC 10 In distribution
P864572 In distribution
NON21430CC 10 In distribution
MDS71757 5 In distribution
PRM21430LF 10 In distribution
DNSCTM25432 In distribution
NON21449XR 1,280 In distribution
BNS119383 100 In distribution
MDS73512 5 In distribution
PRM21438LF In distribution
DNSCTMX05230 800 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
AMD-Ritmed AMD Medicom Inc. 248
DeRoyal Deroyal Industries, Inc. 172
Situate Covidien LP 60
Medical Action Industries Medical Action Industries, Inc. 58
SurgiCount Safety-Sponge Stryker GmbH 50
Dermapac, Inc. Dermapac Inc. 48
Surgicount Stryker GmbH 48
Dukal Dukal LLC 46
ORLocate Steris Corporation 35
A Plus A Plus International, Inc 33
Pilling Teleflex Medical LLC 31
Fabco First AID Bandage Co Inc 27

Showing 12 of 82. All products under Gauze/Sponge, Internal, X-Ray Detectable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K771395 1977-08-19

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