Shandong Dermcosy Medical Supplies Co., Ltd.

FDA Device Registration & Listing · Zibo City Shandong, CN · Registration 3005030934

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
3005030934
FEI Number
3005030934
Entity Name
Shandong Dermcosy Medical Supplies Co., Ltd.
City/State/Country
Zibo City Shandong, CN
Establishment Address
East Area, 3rd Floor, Building 7, Phase 4, Huahong Publishing Technology Industrial Park, No. 7 Minxiang North Road, New High-tech Industrial Development Zone,, Zibo City Shandong 255000, CN
Establishment Type(s)
Sterilize Medical Device for Another Party (Contract Sterilizer),Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Shandong Dermcosy Medical Supplies Co., Ltd. (Owner Number: 9070541)
Owner / Operator Contact Address
East Area, 3rd Floor, Building 7, Phase 4, Huahong Publishing Technology Industrial Park, No. 7 Minxiang North Road, New High-tech Industrial Development Zone,, Zibo City, CN-SD 255000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dressing, Wound, Hydrophilic Gauze/Sponge Tape and Bandage, Adhesive

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2005-02-17
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2005-02-17
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2005-02-17

Official Correspondent

Chris Song

US Agent Details

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

Related Public Records

Same Entity

Shandong Dermcosy Medical Supplies 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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005030934. Last updated year: 2026. Please use registration number 3005030934 when referencing this establishment in official correspondence.
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