Data / Medical devices / United States / Luminance Medical Ventures Incorporated
Luminance Medical Ventures Incorporated: FDA-registered device maker in The Colony, TX, United States, 2 510(k) clearances
Luminance Medical Ventures Incorporated is registered with the FDA (registration 3020491484) in The Colony, TX, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 23, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3020491484
- Address
- 5752 Grandscape Blvd Ste 225, The Colony, TX, United States, 75056
- Owner or operator
- Luminance Medical Ventures Incorporated (10082015)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- September 24, 2021
- Registered through
- 2027
- Brand names listed
- Luminance RED, Luminance RED Acne Device, Luminance RED Cold Sore Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Light Based Treatment For Cold Sores Herpes Simplex Virus-1 | OKJ | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| September 23, 2025 | K251973 | Luminance Red Cold Sore Device (TN1927G) | OKJ | Substantially Equivalent | Luminance Medical Ventures, Inc. | accessdata.fda.gov |
| June 9, 2022 | K220729 | The Luminance RED Acne Device | OLP | Substantially Equivalent | Luminance Medical Ventures, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Lamp, Infrared, Therapeutic Heating
Updated September 23, 2025. 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.