FDA Record: MAJESTY-TECH PRODUCT DEVELOPMENT CORP. (1000109362)

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000109362

FEI Number

1000109362

Entity Name

MAJESTY-TECH PRODUCT DEVELOPMENT CORP.

City/State/Country

Taipei City, TW

Establishment Address

Rome 1307, 13F., No. 333, Sec. 1, Keelung Road, Xinyi Dist., Taipei City 11012, TW

Establishment Type(s)

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

Owner / Operator

Majesty-Tech Product Development Corp. (Owner Number: 10056291)

Owner / Operator Contact Address

Rome 1307, 13F., No. 333, Sec. 1, Keelung Road, Xinyi Dist., Taipei City, TW-TPE 11012, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pelvic Support

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISR	Band Or Belt, Pelvic Support	Physical Medicine	Class 1	890.3025	2017-11-25

Official Correspondent

No official correspondent registered.

US Agent Details

Shu-Chen Cheng Business: ROC Chinese-European Industrial Research Society Email: ceirs.jen@msa.hinet.net Phone: (614) 5888168

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000109362. Last updated year: 2026. Please use registration number 1000109362 when referencing this establishment in official correspondence.