Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013423303

FEI Number

3013423303

Entity Name

KAERTECH ELECTRONICS PHILIPPINES INC

City/State/Country

Binan Laguna, PH

Establishment Address

Building 3, EZP Compound, Laguna Technopark Annex, Binan Laguna 4024, PH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Kaertech Limited (Owner Number: 10052737)

Owner / Operator Contact Address

Unit 15 6/F, Hong Kong Plaza, 188 Connaught Road West, Kennedy Town, HK-NOTA 000, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

upLift 5

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2024-10-06
OHS	Light Based Over The Counter Wrinkle Reduction	General, Plastic Surgery	Class 2	878.4810	2025-09-10
OLP	Over-The-Counter Powered Light Based Laser For Acne	General, Plastic Surgery	Class 2	878.4810	2025-09-10

Official Correspondent

Marjorie Cuevas

US Agent Details

Mathew John Business: Kaertech Inc Email: quality@kaertech.com Phone: (212) 9830890

Related Public Records

Same Entity

Kaertech Limited

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013423303. Last updated year: 2026. Please use registration number 3013423303 when referencing this establishment in official correspondence.