Data / Medical devices / United States / Microlight Corporation Of America
Microlight Corporation Of America: FDA-registered device maker in Missouri City, TX, United States, 2 510(k) clearances
Microlight Corporation Of America is registered with the FDA (registration 3003654318) in Missouri City, TX, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 3, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003654318
- Address
- 3634 Glenn Lakes Ln Ste 243, Missouri City, TX, United States, 77459
- Owner or operator
- MICROLIGHT CORPORATION OF AMERICA (9049695)
- Roles
- Specification developer
- First device listed
- December 21, 2007
- Registered through
- 2026
- Brand names listed
- ML 830 Laser, MicroLight Smart Laser
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Specification developer | accessdata.fda.gov |
| Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy | NHN | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 3, 2008 | K080786 | ML830TP | ILY | Substantially Equivalent | Microlight Corporation of America | accessdata.fda.gov |
| February 6, 2002 | K010175 | MICROLIGHT 830 LASER SYSTEM | NHN | Substantially Equivalent | Microlight Corporation of America | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
- All makers of Lamp, Infrared, Therapeutic Heating
Updated October 3, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.