Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016711531

FEI Number

3016711531

Entity Name

BRANCH IN PHU THO, THYGESEN TEXTILE VIETNAM COMPANY LIMITED

City/State/Country

Yen Lap Commune Phu Tho, VN

Establishment Address

Chua 11 Village,, Yen Lap Commune Phu Tho 35500, VN

Establishment Type(s)

Remanufacture Medical Device,Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

BRANCH IN PHU THO, THYGESEN TEXTILE VIETNAM COMPANY LIMITED (Owner Number: 10093500)

Owner / Operator Contact Address

Chua 11 Village,, Yen Lap Commune,, VN-68 35500, VN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Miracle Back Relief 12 PC Master Miracle Headache Relief 12 PC Master Miracle Knee Relief 12 PC Master Miracle Arch Relief 12 PC Master Miracle Foot Relief 12 PC Master Miracle Miracle Eye Relief 12 PC Master Gel RX 12 PC Master (Headache Relief All Black)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2025-05-26

Official Correspondent

No official correspondent registered.

US Agent Details

Wen Wang Business: Willow Glen Consultancy LLC Email: Wen.Wang@WillowGlenFDA.com Phone: (619) 8690249

Related Public Records

Same Entity

BRANCH IN PHU THO, THYGESEN TEXTILE VIETNAM COMPANY LIMITED

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

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3008384548	ACTIVE-ICE, INC.	Norman, OK, US
3002393819	MEDICAL SPECIALTIES OF CALIFORNIA LIMITED	Orpington Kent, GB
3038195249	SHENZHEN KADUO INDUSTRIAL CO., LTD	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016711531. Last updated year: 2026. Please use registration number 3016711531 when referencing this establishment in official correspondence.