Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014128876

FEI Number

3014128876

Entity Name

LIDLIFT, LLC

City/State/Country

West Valley City, UT, US

Establishment Address

2943 Parkway Blvd, PMB 125, West Valley City, UT 84119, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

LidLift, LLC (Owner Number: 10056167)

Owner / Operator Contact Address

2943 Parkway Blvd, PMB 125, West Valley City, UT 84119, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LidLiftGoggle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2017-11-11

Official Correspondent

John McCann

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LidLift, LLC

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 3014128876. Last updated year: 2026. Please use registration number 3014128876 when referencing this establishment in official correspondence.