PDS Optical Florida

FDA Device Registration & Listing · Fort Lauderdale, FL, US · Registration 3017296478

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
3017296478
FEI Number
3017296478
Entity Name
PDS Optical Florida
City/State/Country
Fort Lauderdale, FL, US
Establishment Address
5353 NW 35th Ave, Fort Lauderdale, FL 33309, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PDS Optical (Owner Number: 10090102)
Owner / Operator Contact Address
3801 Bishop Lane, Louisville, KY 40218, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kamber Lens Factory Kamber Lens Factory Lens Factory Kamber Kamber Lens Factory Eagle Safety Lens Factory Kamber

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2024-02-15
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2024-02-15
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2024-02-15
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2024-02-15
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2024-02-15

Official Correspondent

Bill Dufort

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PDS Optical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3030643434 PDS OPTICAL Louisville, KY, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017296478. Last updated year: 2026. Please use registration number 3017296478 when referencing this establishment in official correspondence.
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