FOSHAN AQUA GEL BIOTECH CO. LTD.

FDA Device Registration & Listing · Foshan Guangdong, CN · Registration 3007222546

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
3007222546
FEI Number
3007222546
Entity Name
FOSHAN AQUA GEL BIOTECH CO. LTD.
City/State/Country
Foshan Guangdong, CN
Establishment Address
Jili Industrial Park, Qiaole Road, Nanzhuang Town Chancheng District, Foshan Guangdong 528000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Foshan Aqua Gel Biotech Co. Ltd. (Owner Number: 10026638)
Owner / Operator Contact Address
Jill Industrial Park, Qiaole Road, Nanzhuang Town, Chancheng District, Foshan, CN-GD CN-44, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Hot Warming Pad Guaze Tape and bandage, adhesive Patch on Skin Warm Pad Cooling Gel Mat Cool Bandage Chill Cool Pad Cool and Hot Gel Pad

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IMA Pack, Heat, Moist Physical Medicine Class 1 890.5730 2010-12-01
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2009-11-07
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2013-04-25
OMW Adhesive Backed Thermal Skin Patches Physical Medicine Class 1 890.5710 2010-12-01
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2010-12-01

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

Foshan Aqua Gel Biotech 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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3003079019 KOBAYASHI AMERICA MANUFACTURING, LLC Dalton, GA, US
3011182985 Kunshan Topgel Industry Co., Ltd Kunshan Jiangsu, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007222546. Last updated year: 2026. Please use registration number 3007222546 when referencing this establishment in official correspondence.
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