Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1063300

FEI Number

1000488948

Entity Name

PROTECH LEADED EYEWEAR, INC.

City/State/Country

West Palm Beach, FL, US

Establishment Address

7960 Central Industrial Drive, Ste 125, West Palm Beach, FL 33404, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Protech Leaded Eyewear, Inc. (Owner Number: 10025412)

Owner / Operator Contact Address

7960 Central Industrial Drive, Ste 125, West Palm Beach, FL 33404, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Protech Leaed Eyewear Inc. Prolite IEC Proguard Apron Apollo Apron Nano Prolite Bilayer IEC Premier

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IWX	Barrier, Control Panel, X-Ray, Movable	Radiology	Class 1	892.6500	2008-04-14
IWO	Apron, Protective	Radiology	Class 1	892.6500	2008-04-14

Official Correspondent

Evin Lalan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Protech Leaded Eyewear, Inc.

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 1063300. Last updated year: 2026. Please use registration number 1063300 when referencing this establishment in official correspondence.