Sebacia, Inc.
Country not established
- Devices
- 2
What Sebacia, Inc. makes
Sebacia, Inc. manufactures photothermal therapy gels designed for targeted skin treatments, including Sebacia Microparticles, which are formulated for localized thermal effects on acne-prone or hyperkeratotic skin.
The company’s products are regulated as Class II medical devices in the US, with authorisations supported by FDA 510(k) and UDI listings. The company is headquartered in the United States.
Catalogue
- Registry: GUDID
Sebacia Microparticles Ref K181518
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 963219600
- [email protected]
- Phone
- 6788121138
Frequently asked questions
How many devices does Sebacia, Inc. have in the registry?
The registry currently lists 2 devices for Sebacia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sebacia, Inc.'s devices?
Among its 2 most recently registered devices, Sebacia, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Sebacia, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sebacia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sebacia, Inc. in the registry?
The most recently registered devices listed for Sebacia, Inc. include Sebacia Microparticles SEB-250-3P-US and Sebacia Microparticles.