Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019039128

FEI Number

3019039128

Entity Name

B&A PRECISION SILICONE RUBBER (DONGGUAN) CO., LTD

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Rm. 201, No. 5 Wulian Gongye 1st Rd, Fenggang Town, Dongguan Guangdong 523695, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

B&A Precision Silicone Rubber (Dongguan) Co., Ltd (Owner Number: 10081771)

Owner / Operator Contact Address

Rm. 201, No. 5 Wulian Gongye 1st Rd, Fenggang Town, Dongguan, CN-GD 523682, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Breast Pump Accessory, Milk Expression Aid, via Positive Pressure Sizing inserts (15mm, 17mm, 19mm),Fitment Assembly - Umbrella valves Reia Pessary Reia Applicator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PWA	Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure	Obstetrics/Gynecology	Class 1	884.5150	2021-05-13
HFS	Shield, Nipple	General Hospital	Class 1	880.5630	2021-07-26
HHW	Pessary, Vaginal	Obstetrics/Gynecology	Class 2	884.3575	2024-07-05
HGD	Applicator, Vaginal	Obstetrics/Gynecology	Class 1	884.4520	2024-07-05

Official Correspondent

Fuqin Yang

US Agent Details

shally dream Email: mljyangguang@msn.com Phone: (909) 2820679

Related Public Records

Same Entity

B&A Precision Silicone Rubber (Dongguan) 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
K933654	Johnson & Johnson Medical, Inc.	BLADDER NECK SUPPORT PROTHESIS FITTING KIT	1995-05-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019039128. Last updated year: 2026. Please use registration number 3019039128 when referencing this establishment in official correspondence.