Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031656500

FEI Number

3031656500

Entity Name

LensAdvisor Lab

City/State/Country

Ammon, ID, US

Establishment Address

1231 Trappers Rdg, Ammon, ID 83401, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

LensAdvisor (Owner Number: 10094754)

Owner / Operator Contact Address

7 Ann Siang Hill 02-01, Singapore, SG-01 069791, SG

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LensAdvisor Prescription Lenses

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2025-12-20

Official Correspondent

Zenos Schmickrath

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LensAdvisor

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3006755718	DONGGUAN YUEHENG OPTICAL CO. LTD.	Dongguan Guangdong, CN
3015534032	BOLLE SAFETY INC	Carlsbad, CA, US
3007675955	Carl Zeiss Vision Canada, Inc.	Toronto Ontario, CA
1000428458	GKB OPHTHALMICS LIMITED - UNIT II	North Goa Goa, IN
3038136215	MEIVISION (VIETNAM) CO., LTD	Ho Chi Minh City, VN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031656500. Last updated year: 2026. Please use registration number 3031656500 when referencing this establishment in official correspondence.