Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016170587

FEI Number

3016170587

Entity Name

TIANJIN HODAF TECHNOLOGY CO., LTD.

City/State/Country

TIANJIN, CN

Establishment Address

2-601 CHENYING BUILDING, XINKAI ROAD, HEDONG DISTRICT, TIANJIN 300011, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Tianjin Hodaf Technology Co., Ltd. (Owner Number: 10092797)

Owner / Operator Contact Address

2-601 CHENYING BUILDING, XINKAI ROAD, HEDONG DISTRICT, TIANJIN, CN-NOTA 300011, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Nasal Inhaler Foot Patch, Foot Mask, Slimming Patch, Health Patch, Mouth Tape, Adhesive Patch, Hand Mask, Face Tape Menstrual Relief Patch, Forehead Patch Nasal/Nose Patch/Strips, Transdermal Patch Hydrocolloid Patches, Hydrocolloid Roll Scar Sheet Wrinkle Patches Silicone Tape Silicone Patch Wrist Warmer Patch, Belly Warmer Patch, Chin Patch, Knee Patch, Neck Patch, Eye Patch, Sun Patch, Cool Patch Hot Cold Disposable Pack, Pain Relief Patch, Warm Patch, Steam Eye Mask/Patch, Hand Warmer Patch Foot Warmer Patch, Body Warmer Patch, Neck Warmer Patch, Waist Warmer Patch, Knee Warmer Patch

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2025-08-12
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2025-08-12
OMW	Adhesive Backed Thermal Skin Patches	Physical Medicine	Class 1	890.5710	2025-08-12
LWF	Dilator, Nasal	Ear, Nose, Throat	Class 1	874.3900	2025-08-12
NAE	Dressing, Wound, Hydrogel Without Drug And/Or Biologic	General, Plastic Surgery	Class 1	878.4022	2025-08-12
MDA	Elastomer, Silicone, For Scar Management	General, Plastic Surgery	Class 1	878.4025	2025-02-19
IMD	Pack, Hot Or Cold, Disposable	Physical Medicine	Class 1	890.5710	2025-08-12

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

Tianjin Hodaf Technology 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
K880871	John Wagner Associates, Inc.	GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER	1988-05-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0505-2022	Philips North America Llc	1	Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022	Philips North America Llc	1	Infant Heel Warmers w/strap, Reference # 989805603201 1223

Similar Registrations

Registration Number	Establishment Name	Location
3033571062	MERZ PHARMACEUTICALS, LLC	Raleigh, NC, US
1526711	ISOMEDIX OPERATIONS INC	GROVEPORT, OH, US
3010200299	Foundation Consumer Healthcare	Pittsburgh, PA, US
3021011196	E-LINKCARE MEDITECH CO., LTD.	Taizhou Zhejiang, CN
3012896103	SHENZHEN BALINDA TECHNOLOGY CO.,LTD	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016170587. Last updated year: 2026. Please use registration number 3016170587 when referencing this establishment in official correspondence.