ZHEJIANG B.M. INDUSTRIAL CO., LTD.

FDA Device Registration & Listing · Huzhou Zhejiang, CN · Registration 3027320369

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3027320369
FEI Number
3027320369
Entity Name
ZHEJIANG B.M. INDUSTRIAL CO., LTD.
City/State/Country
Huzhou Zhejiang, CN
Establishment Address
No. 58 WUNIUSHAN ROAD, QIANYUAN, DEQING, Huzhou Zhejiang 313216, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
ZHEJIANG B.M. INDUSTRIAL CO., LTD. (Owner Number: 10088663)
Owner / Operator Contact Address
No. 58 WUNIUSHAN ROAD, QIANYUAN, DEQING, Huzhou, CN-ZJ 313216, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BLADDER LINER PAD Incontinence pads Men Incontinence Pads, Men PROTECTIVE SHIELD, Men Incontinence Guards, 210, 255, 290 Panty Liner; Sanitary Napkin, INCONTINENCE PADS Panty Liner; Sanitary Napkin, INCONTINENCE PADS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2023-09-26
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2023-09-26
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2023-09-26

Official Correspondent

SHUFENG DING

US Agent Details

James St WU Business: Humiss Inc. Email: fda-reg@humiss.com Phone: (720) 7595888

Related Public Records

Same Entity

ZHEJIANG B.M. INDUSTRIAL 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

Similar Registrations

Registration Number Establishment Name Location
3032900656 CAREWELL FAMILY, INC Coral Gables, FL, US
3011446173 FISCHER MANUFACTURING LLC Fairfield, OH, US
3010048541 ABENA NORTH AMERICA, INC. Oceanside, CA, US
3016452317 GUANGDONG CHUANTIAN SANITARY PRODUCTS CO.,LTD Zhongshan Guangdong, CN
3012162353 INTELLIGENT FABRIC TECHNOLOGIES (NORTH AMERICA) INC. Markham Ontario, CA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027320369. Last updated year: 2026. Please use registration number 3027320369 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.