THREE RIVERS OPTICAL

FDA Device Registration & Listing · Pittsburgh, PA, US · Registration 3002653402

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
3002653402
FEI Number
3002653402
Entity Name
THREE RIVERS OPTICAL
City/State/Country
Pittsburgh, PA, US
Establishment Address
260 Bilmar Dr, Pittsburgh, PA 15205, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device,Reprocess Single-Use Device
Owner / Operator
three rivers optical (Owner Number: 10093584)
Owner / Operator Contact Address
260 bilmar dr, Pittsburgh, PA 15205, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

IDOC frames idoc lenses

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2025-06-06
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2026-01-22

Official Correspondent

steven seibert

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

three rivers optical
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 3002653402. Last updated year: 2026. Please use registration number 3002653402 when referencing this establishment in official correspondence.
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