Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043138901

FEI Number

3043138901

Entity Name

DONGGUAN SAMVO BIOTECHNOLOGY CO., LTD

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Room 501, Building 1, No. 112, Bihu Avenue, Fenggang Town, Dongguan City, Guangdong Province, Dongguan Guangdong 523000, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Dongguan samvo Biotechnology Co., Ltd (Owner Number: 10094765)

Owner / Operator Contact Address

Room 501, Building 1, No. 112, Bihu Avenue, Fenggang Town, Dongguan City, Guangdong Province, Dongguan, CN-GD 523000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Silicone gel patch Silicone scar patch Heel patch Mosquito repellent patch Sports tape Pu Film Roll Adhesive patch Anti- snoring Strip Quit smoking patch Kinesiology tape Sleep patch Band-Aid Mouth tape Nasal strip Medical Dressings Fungal nail patches Facial lifting patch Hydrocolloid pimple Patch Acne patch Hydrocolloid patch Hydrocolloid roll

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	2025-12-22
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2025-12-22
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2025-12-22

Official Correspondent

Chen Zhenyang

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Dongguan samvo Biotechnology 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
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

Similar Registrations

Registration Number	Establishment Name	Location
2950792	BIODERMIS LLC	Henderson, NV, US
3009192857	Neodyne Biosciences, Inc.	Fremont, CA, US
3005857283	PRECO, LLC	Somerset, WI, US
3019769561	ScarPro NV	Aalter Flanders, BE
1062964	Atlantic Medical Products, LLC	Saint Petersburg, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043138901. Last updated year: 2026. Please use registration number 3043138901 when referencing this establishment in official correspondence.