Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014627088

FEI Number

3014627088

Entity Name

HONG KONG OPTICAL LENS PHILS. LABORATORY INC.

City/State/Country

Quezon City National Capital Region, PH

Establishment Address

#74 Mindanao Ave., Proj. 6, Quezon City National Capital Region 1100, PH

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Hong Kong Optical Lens Phils. Laboratory Inc. (Owner Number: 10060649)

Owner / Operator Contact Address

#74 Mindanao Ave., Proj. 6, Quezon City, PH-00 1100, PH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

APOLLO APOLLO APOLLO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2019-06-06
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2019-06-06
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2019-06-06

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

Hong Kong Optical Lens Phils. Laboratory Inc.

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
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014627088. Last updated year: 2026. Please use registration number 3014627088 when referencing this establishment in official correspondence.