MENTRA LABS INC

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3036367365

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3036367365
FEI Number
3036367365
Entity Name
MENTRA LABS INC
City/State/Country
San Francisco, CA, US
Establishment Address
369 Hayes St, San Francisco, CA 94102, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Mentra Labs Inc (Owner Number: 10094967)
Owner / Operator Contact Address
369 Hayes Street, San Francisco, CA 94102, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mentra Live Mentra Nex

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2026-01-11

Official Correspondent

Saranda Halitaj

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mentra Labs 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 3036367365. Last updated year: 2026. Please use registration number 3036367365 when referencing this establishment in official correspondence.
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