ART CRAFT OPTICAL CO., INC.

FDA Device Registration & Listing · Rochester, NY, US · Registration 1317330

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
1317330
FEI Number
1317330
Entity Name
ART CRAFT OPTICAL CO., INC.
City/State/Country
Rochester, NY, US
Establishment Address
57 Goodway Drive South, Rochester, NY 14623, US
Establishment Type(s)
Repack or Relabel Medical Device,Remanufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Art Craft Optical Co., Inc. (Owner Number: 10035954)
Owner / Operator Contact Address
57 Goodway Drive South, Rochester, NY 14623, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ArtCraft Sunglasses ArtCraft Optical

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2018-02-14
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2014-01-22

Official Correspondent

Hassan Tariq

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Art Craft Optical Co., 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
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12
K970895 Custom Optical Frames, Inc. CUSTOM OPTICAL SUNGLASS FRAMES 1997-05-06
K853921 Winsburn Company , Ltd. ALL KINDS OF SUNGLASSES 1985-10-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1317330. Last updated year: 2026. Please use registration number 1317330 when referencing this establishment in official correspondence.
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