WEARME PRO

FDA Device Registration & Listing · Scottsdale, AZ, US · Registration 3013659124

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
3013659124
FEI Number
3013659124
Entity Name
WEARME PRO
City/State/Country
Scottsdale, AZ, US
Establishment Address
7575 E Redfield Rd Ste 125, Scottsdale, AZ 85260, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
WearMe Pro (Owner Number: 10055127)
Owner / Operator Contact Address
7575 E REDFIELD RD, UNIT 125, Scottsdale, AZ 85260, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

WMP Eyewear

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 2025-11-16

Official Correspondent

David Bozek

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WearMe Pro
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 3013659124. Last updated year: 2026. Please use registration number 3013659124 when referencing this establishment in official correspondence.
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