GUANGXI DEZHIRAN BIOTECHNOLOGY CO., LTD.

FDA Device Registration & Listing · nanning Guangxi, CN · Registration 3033891906

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
3033891906
FEI Number
3033891906
Entity Name
GUANGXI DEZHIRAN BIOTECHNOLOGY CO., LTD.
City/State/Country
nanning Guangxi, CN
Establishment Address
Room 202, North Side 2nd Floor,Building A1,Nanning Ecological Industrial Park,No. 110 Zhenxing Road, Xixiangtang District, nanning Guangxi 530000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Guangxi Dezhiran Biotechnology Co., LTD. (Owner Number: 10091874)
Owner / Operator Contact Address
Room 202, North Side 2nd Floor,Building A1,Nanning Ecological Industrial Park,No. 110 Zhenxing Road,, Xixiangtang District, nanning, CN-GX 530000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

silicone scar sheet Waterproof Silicone Sheet Waterproof Ear Covers Waterproof Silicone Patch Silicone Sports Tape silicone medical tape Medical waterproof silicone band-aid Waterproof Tattoo Patch

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 2024-11-11
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2024-11-11

Official Correspondent

Manyi Chen

US Agent Details

hui hong Business: ABMED MEDICAL TECHNOLOGY INC Email: info@abmed.us Phone: (509) 5816099

Related Public Records

Same Entity

Guangxi Dezhiran 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

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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 3033891906. Last updated year: 2026. Please use registration number 3033891906 when referencing this establishment in official correspondence.
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