Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008297535

FEI Number

3008297535

Entity Name

UNI PRECISION INDUSTRIAL LTD.

City/State/Country

Kowloon, HK

Establishment Address

Room 1303, Tower 1, Harbour Centre, 1 Hok Cheung, Hunghom, Kowloon None, HK

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

UNI Precision Industrial Ltd. (Owner Number: 10052746)

Owner / Operator Contact Address

Room 1303, Tower 1, Harbour Centre, 1 Hok Cheung, Hunghom, Kowloon, HK-NOTA None, 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
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2020-12-24

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

UNI Precision Industrial 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
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008297535. Last updated year: 2026. Please use registration number 3008297535 when referencing this establishment in official correspondence.