Revelle Aesthetics, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Revelle Aesthetics, Inc. makes
Revelle Aesthetics, Inc. manufactures devices for aesthetic treatments, including manual cutters designed to disrupt cellulite fibrous tethers and transilluminators for subcutaneous infusion procedures. Their portfolio includes branded systems like Aveli and Alite, which target skin texture and tissue treatment.
The company’s devices are regulated under FDA classifications, with some falling under Class I and others under Class II. They are listed in the FDA’s 510(k) and UDI registries, reflecting their authorised status in the US market.
Catalogue
Company details
- DUNS number
- 117419977
Frequently asked questions
How many devices does Revelle Aesthetics, Inc. have in the registry?
The registry currently lists 5 devices for Revelle Aesthetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Revelle Aesthetics, Inc.'s devices?
Among its 5 most recently registered devices, Revelle Aesthetics, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Revelle Aesthetics, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Revelle Aesthetics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Revelle Aesthetics, Inc. in the registry?
The most recently registered devices listed for Revelle Aesthetics, Inc. include Aveli AVE002, Alite AVE003, Aveli AVE001 and Avéli.