Envis, Inc.
Country not established
- Devices
- 1
What Envis, Inc. makes
Envis, Inc. manufactures the AROMAPATCH, a transdermal delivery system designed for the administration of aromatherapy compounds through the skin. This device is intended for non-invasive topical application, providing controlled release of essential oils or fragrance agents.
The AROMAPATCH falls under FDA Class I regulatory classification and is listed via the 510(k) pathway. The company is based in the United States, where its devices are subject to U.S. regulatory requirements.
Catalogue
Aromapatch Ref K984345
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Envis, Inc. have in the registry?
The registry currently lists 1 device for Envis, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Envis, Inc.'s devices?
Among its 1 most recently registered device, Envis, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Envis, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Envis, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Envis, Inc. in the registry?
The most recently registered devices listed for Envis, Inc. include AROMAPATCH.