Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009773371

FEI Number

3009773371

Entity Name

JT TECH ELECTRONICS (HONG KONG) CO LTD

City/State/Country

Hong Kong, HK

Establishment Address

Unit 210 of the 2nd Floor of Building 8W, Phase Two,, Hong Kong Science Park, Pak Shek Kok, New Territories,, Hong Kong No ZidCode, HK

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

JT Tech Electronics (Hong Kong) Co Ltd (Owner Number: 10041803)

Owner / Operator Contact Address

Unit 210 of the 2nd Floor of Building 8W, Phase Two,, Hong Kong Science Park, Pak Shek Kok, New Territories,, Hong Kong, HK-NOTA No ZipCode, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DSA	Cable, Transducer And Electrode, Patient, (Including Connector)	Cardiovascular	Class 2	870.2900	2019-06-28
DSA	Cable, Transducer And Electrode, Patient, (Including Connector)	Cardiovascular	Class 2	870.2900	2017-02-22

Official Correspondent

Victor Pau

US Agent Details

Gilbert T Sommer Email: gtreacysommer@gmail.com Phone: (858) 4052740

Related Public Records

Same Entity

JT Tech Electronics (Hong Kong) 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
K880323	Medtronic Vascular	MEDTRONIC MODEL 5411 SURGICAL CABLE ADAPTOR	1988-03-22

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3017636737	STERIS Corporation de Republica Dominicana, S.R.L.	Santo Domingo, DO
3004859241	BOSTON SCIENTIFIC CORPORATION	La Aurora Heredia, CR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009773371. Last updated year: 2026. Please use registration number 3009773371 when referencing this establishment in official correspondence.