Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008111543

FEI Number

3008111543

Entity Name

AAB (CHINA) CO., LTD.

City/State/Country

Nanan City Fujian, CN

Establishment Address

AAB Industrial Park, HONGLAI TOWN, Nanan City Fujian 362331, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

AAB (CHINA) CO., LTD. (Owner Number: 10031023)

Owner / Operator Contact Address

AAB Industrial Park, HONGLAI TOWN, Nanan City, CN-FJ 362331, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sanitary Napkin Panty Liner Incontinent Pad KN 95 Respirators KN 95 Masks Isolation Mask

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2009-12-10
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2012-03-04
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2012-03-04
MSH	Respirator, Surgical	General, Plastic Surgery	Class 2	878.4040	2020-04-12
KHA	Mask, Scavenging	Anesthesiology	Class 1	868.5590	2020-04-12

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Shen Business: Manton Business and Technology Services Email: cyshen@aol.com Phone: (608) 2179358

Related Public Records

Same Entity

AAB (CHINA) CO., LTD.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K823241	Kimberly-Clark Corp.	NEW FREEDOM THIN UNSCENTED MAXI PADS	1982-12-28
K102092	Prestige Ameritech	PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES	2010-10-06

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3017366514	FIBRIL TEX PVT LTD.	Amritsar Punjab, IN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008111543. Last updated year: 2026. Please use registration number 3008111543 when referencing this establishment in official correspondence.