Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005595143

FEI Number

3005595143

Entity Name

FEA INDUSTRIES, INC.

City/State/Country

Morton, PA, US

Establishment Address

1 North Morton Ave, Morton, PA 19070, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

FEA Industries, Inc. (Owner Number: 10053266)

Owner / Operator Contact Address

1 North Morton Ave., Morton, PA 19070, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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	2016-11-15

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FEA Industries, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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3007675955	Carl Zeiss Vision Canada, Inc.	Toronto Ontario, CA
1000428458	GKB OPHTHALMICS LIMITED - UNIT II	North Goa Goa, IN
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005595143. Last updated year: 2026. Please use registration number 3005595143 when referencing this establishment in official correspondence.