Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010256218

FEI Number

3010256218

Entity Name

BENQ MATERIALS CORPORATION

City/State/Country

Gueishan Taoyuan, TW

Establishment Address

29, Jianguo E. Rd., Gueishan Taoyuan 333403, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BENQ MATERIALS CORPORATION (Owner Number: 10044989)

Owner / Operator Contact Address

29, Jianguo E. Rd., Gueishan, TW-TAO 333, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AnsCare Scar Reduction Silicone Gel C+ AnsCare LeniScar Silicone Stick Anscare SIMO Negative Pressure Wound Therapy (NPWT) System StatGuard Hemostatic Dressing StatGuard Hemostatic Patch AnsCare Hydrocolloid Dressing (Sterile)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MDA	Elastomer, Silicone, For Scar Management	General, Plastic Surgery	Class 1	878.4025	2014-01-23
OKO	Negative Pressure Wound Therapy Non-Powered Suction Apparatus	General, Plastic Surgery	Class 2	878.4683	2020-05-07
QSY	Hemostatic Wound Dressing Without Thrombin Or Other Biologics	Unknown	Class U	N/A	2015-04-13
QSY	Hemostatic Wound Dressing Without Thrombin Or Other Biologics	Unknown	Class U	N/A	2018-12-18
NTC	Nursing Pad, Hydrogel	General Hospital	Class 1	880.5630	2024-10-28
NAE	Dressing, Wound, Hydrogel Without Drug And/Or Biologic	General, Plastic Surgery	Class 1	878.4022	2018-04-25

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

BENQ MATERIALS CORPORATION

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
K113032	Spiracur, Inc.	SNAP WOUND CARE SYSTEM	2011-12-01
K220566	Koag, LLC	Vascette HP (hemostatic pad)	2022-07-29
K080818	Hem Con Medical Technologies, Inc.	HEMCON BANDAGE, HEMCON BANDAGE OTC, HEMCON CHITOFLEX-SURGICAL DRESSING	2008-05-15
K893123	Les Laboratorires Brothier, S.A.	ADHESIVE BANDAGES & PADS FOR MINOR CUTS/SCRAPES	1990-02-13
K143462	Benq Materials Corporation	AnsCare ChitoClot Gauze (prescription use), AnsCare ChitoClot Gauze (over-the-counter use)	2015-05-08

Similar Registrations

Registration Number	Establishment Name	Location
2950792	BIODERMIS LLC	Henderson, NV, US
3043138901	DONGGUAN SAMVO BIOTECHNOLOGY CO., LTD	Dongguan Guangdong, CN
3009192857	Neodyne Biosciences, Inc.	Fremont, CA, US
3005857283	PRECO, LLC	Somerset, WI, US
3019769561	ScarPro NV	Aalter Flanders, BE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010256218. Last updated year: 2026. Please use registration number 3010256218 when referencing this establishment in official correspondence.