Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1037039

FEI Number

1037039

Entity Name

QED, INC.

City/State/Country

LEXINGTON, KY, US

Establishment Address

750 ENTERPRISE DR., LEXINGTON, KY 40510, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

QED, INC. (Owner Number: 1037039)

Owner / Operator Contact Address

750 ENTERPRISE DR., --, Lexington, KY 40510, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

C3 Portable LED Headlight System C3 Portable LED Headlight System Beamer LED Light Source Nova 300 Altair HI2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HPP	Headlamp, Operating, Battery-Operated	Ophthalmic	Class 1	886.4335	1992-11-23
FTD	Lamp, Surgical	General, Plastic Surgery	Class 2	878.4580	2007-11-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

QED, 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 1037039. Last updated year: 2026. Please use registration number 1037039 when referencing this establishment in official correspondence.