Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015781786

FEI Number

3015781786

Entity Name

ALLMED MEDICAL PRODUCTS CO., LTD. -JIANLI

City/State/Country

Jingzhou Hubei, CN

Establishment Address

No. 168-1(Te), Yusha Road, Rongcheng Town, Jianli County, Jingzhou Hubei 433300, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

ALLMED MEDICAL PRODUCTS CO., LTD. (Owner Number: 9033718)

Owner / Operator Contact Address

No.18 Qixing Road, Majiadian Town, Zhijiang City, CN-HB 443200, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Gauze Sponge, X-Ray Detectable Neuro Pads

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2012-02-14
GDY	Gauze/Sponge, Internal, X-Ray Detectable	General, Plastic Surgery	Class 1	878.4450	2006-02-07
NAD	Dressing, Wound, Occlusive	General, Plastic Surgery	Class 1	878.4020	2007-10-29

Official Correspondent

Julia Cheng

US Agent Details

Jessie Yao Business: Medright Tech Inc Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

ALLMED MEDICAL PRODUCTS CO., LTD.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3011862887	ALLMED MEDICAL PRODUCTS CO., LTD.	Zhijiang City Hubei, CN
3011089435	Allmed Industrial Limited	Shenzhen City Guangdong, CN
3004950768	ALLMED MEDICAL PRODUCTS CO., LTD.	ZHIJIANG CITY Hubei, CN

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K790050	Stanford Professional Products	SPONGES, STANFORD STERILE LAP	1979-01-17
K881936	Iberhospitex, S.A.	OPER-FILM-ADHESIVE MEMBRANE	1988-08-31

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2019	COVIDIEN LLC	1	Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.
Z-0014-2019	COVIDIEN LLC	1	Kerlix Bandage Roll, 100% Cotton, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m), REF 6715 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0015-2019	COVIDIEN LLC	1	Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0016-2019	COVIDIEN LLC	1	Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0017-2019	COVIDIEN LLC	1	Dermacea Gauze Fluff Roll, 6 Ply, 4-1/2 x 4-1/8 yd (11.4 cm x 3.7 m), REF 441103 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

Similar Registrations

Registration Number	Establishment Name	Location
3004651943	KURTSAN PHARMACEUTICALS, INC.	Bandirma Balikesir, TR
3012047128	ATHFAR 828, Inc.	Big Rapids, MI, US
3014666579	SHANDONG KANGLI MEDICAL EQUIPMENT TECHNOLOGY CO., LTD.	Zaozhuang Shandong, CN
3007663056	SHANGHAI HUIHU MEDICAL APPLIANCE CO. LTD.	Shanghai, CN
3015068387	GEORGE COUREY INC	Montreal Quebec, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015781786. Last updated year: 2026. Please use registration number 3015781786 when referencing this establishment in official correspondence.