Luminance Medical Ventures, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Luminance Medical Ventures, Inc. makes
Luminance Medical Ventures, Inc. manufactures at-home aesthetic devices, including the Luminance Red Cold Sore Device for localized treatment of cold sores and The Luminance RED Acne Device for acne management. Both products are designed for non-invasive skin therapy using controlled energy delivery.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Luminance Red Cold Sore Device (TN1927G) Ref K251973
Regimes: 510(k) Registry: 510(k)The Luminance RED Acne Device Ref K220729
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luminance Medical Ventures, Inc. have in the registry?
The registry currently lists 2 devices for Luminance Medical Ventures, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luminance Medical Ventures, Inc.'s devices?
Among its 2 most recently registered devices, Luminance Medical Ventures, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Luminance Medical Ventures, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Luminance Medical Ventures, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luminance Medical Ventures, Inc. in the registry?
The most recently registered devices listed for Luminance Medical Ventures, Inc. include Luminance Red Cold Sore Device (TN1927G) and The Luminance RED Acne Device.