Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015176913

FEI Number

3015176913

Entity Name

BRIGHTLAMP, INC

City/State/Country

Indianapolis, IN, US

Establishment Address

1230 Hoyt Ave., Indianapolis, IN 46203, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

brightlamp, INC (Owner Number: 10058974)

Owner / Operator Contact Address

17437 Carey Rd. Box 230, Westfield, IN 46074, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Reflex Pro Reflex Telehealth Reflex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HLG	Pupillometer, Ac-Powered	Ophthalmic	Class 1	886.1700	2018-11-16

Official Correspondent

Kurtis Sluss

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

brightlamp, 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 3015176913. Last updated year: 2026. Please use registration number 3015176913 when referencing this establishment in official correspondence.