Enlitic, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000022843 FEI 3014300962
- Devices
- 4
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- Emergo Europe B.V.NL
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ensight Ref 10005
Regimes: CE MDR Registry: EUDAMEDGUDIDCurie ENDEX Ref 10001
Regimes: CE MDR, withdrawn Registry: EUDAMEDGUDIDStandardize Ref 10004
Regimes: CE MDR, withdrawn Registry: EUDAMEDGUDIDCurie Ref 10000
Regimes: CE MDR, withdrawn Registry: EUDAMEDGUDID
Company details
- EUDAMED SRN
- US-MF-000022843
- FDA FEI number
- 3014300962
- DUNS number
- 081152491
- EUDAMED status
- Active
- EUDAMED registered name
- Enlitic, Inc.
- Registered address
- 1635, Foxtrail Drive, 80538, Loveland, United States
- Website
- www.enlitic.com
- [email protected]
- Phone
- 1-877-365-4842
- PRRC contact
- Treya Collins
Frequently asked questions
How many devices does Enlitic, Inc. have in the registry?
The registry currently lists 4 devices for Enlitic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Enlitic, Inc.'s devices?
Among its 4 most recently registered devices, Enlitic, Inc. has devices listed in EUDAMED (4 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Enlitic, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Enlitic, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Enlitic, Inc. in the registry?
The most recently registered devices listed for Enlitic, Inc. include Ensight, Curie ENDEX, Standardize and Curie.