Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003654318

FEI Number

3003654318

Entity Name

MICROLIGHT CORPORATION OF AMERICA

City/State/Country

Missouri City, TX, US

Establishment Address

3634 Glenn Lakes Ln, Ste 243, Missouri City, TX 77459, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

MICROLIGHT CORPORATION OF AMERICA (Owner Number: 9049695)

Owner / Operator Contact Address

3634 Glenn Lakes Ln, Ste 243, Missouri City, TX 77459, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K010175

PMA Number

N/A

All Registered Proprietary Names

ML 830 Laser

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NHN	Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy	Physical Medicine	Class 2	890.5500	2007-12-21

Official Correspondent

Michael Barbour

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MICROLIGHT CORPORATION OF AMERICA

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 3003654318. Last updated year: 2026. Please use registration number 3003654318 when referencing this establishment in official correspondence.