Encora, Inc.
Country not established
- Devices
- 6
What Encora, Inc. makes
Encora, Inc. manufactures the Encora X1, a medical device designed for [specific application not provided in data]. The product is intended for [purpose not detailed in data], adhering to regulatory standards for its category.
The Encora X1 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is headquartered in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Encora X1 Ref K251517
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 130699159
- [email protected]
- Phone
- 8556995315
Frequently asked questions
How many devices does Encora, Inc. have in the registry?
The registry currently lists 6 devices for Encora, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Encora, Inc.'s devices?
Among its 6 most recently registered devices, Encora, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Encora, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Encora, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Encora, Inc. in the registry?
The most recently registered devices listed for Encora, Inc. include Encora X1 Wristband (S) BND-001 (S), Encora X1 Wristband (M) BND-001 (M), Encora X1 Stimulator STIM-001 and Encora X1 Wristband (L) BND-001 (L).