WAYSON GROUP CO., LTD

FDA Device Registration & Listing · Qingyuan City Guangdong, CN · Registration 3021033324

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
3021033324
FEI Number
3021033324
Entity Name
WAYSON GROUP CO., LTD
City/State/Country
Qingyuan City Guangdong, CN
Establishment Address
No. 1 Zhihui Road, Guangzhou (Qingyuan) Industrial Transfer Zone,Shijiao Town, Qingcheng District, Qingyuan City Guangdong 511545, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
WAYSON GROUP CO., LTD (Owner Number: 10083051)
Owner / Operator Contact Address
No. 1 Zhihui Road, Guangzhou (Qingyuan) Industrial Transfer Zone,Shijiao Town, Qingcheng District, Qingyuan City, CN-GD 511545, 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 DRESSING,WOUND,OCCLUSIVE

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 2021-10-21
NAD Dressing, Wound, Occlusive General, Plastic Surgery Class 1 878.4020 2021-10-21

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

WAYSON GROUP 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
K881936 Iberhospitex, S.A. OPER-FILM-ADHESIVE MEMBRANE 1988-08-31

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2019 COVIDIEN LLC 1
Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.
Z-0014-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100% Cotton, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m), REF 6715 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0015-2019 COVIDIEN LLC 1
Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0016-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0017-2019 COVIDIEN LLC 1
Dermacea Gauze Fluff Roll, 6 Ply, 4-1/2 x 4-1/8 yd (11.4 cm x 3.7 m), REF 441103 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

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3015432652 E.L.F. COSMETICS INC Oakland, CA, US
3043138901 DONGGUAN SAMVO BIOTECHNOLOGY CO., LTD Dongguan Guangdong, CN
3015215566 THE HAIN CELESTIAL GROUP Hoboken, NJ, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021033324. Last updated year: 2026. Please use registration number 3021033324 when referencing this establishment in official correspondence.
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