Candelis, Inc.
United StatesFDA applicant, unverified FDA FEI 3005919188
Candelis, Inc. is a medical device manufacturer, with 177 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 12 Nov 2026.
- Devices
- 177
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 173
- FDA 510(k) 4
- Device classes
- FDA Class II 177
- Identifiers
- FDA FEI 3005919188
- DUNS 079219983
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 177 devicesShowing 1-50 of 177
Company details
- FDA FEI number
- 3005919188
- DUNS number
- 079219983
- Address
- 9903 South Santa Monica Blvd, #2101, Beverly Hills, CA, 90212
- support@candelis.com
- Phone
- 18888008600
Frequently asked questions
How many devices does Candelis, Inc. have in the registry?
The registry currently lists 177 devices for Candelis, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Candelis, Inc.'s devices?
Among its 50 most recently registered devices, Candelis, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Candelis, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Candelis, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Candelis, Inc. in the registry?
The most recently registered devices listed for Candelis, Inc. include ImageGrid StreamVue, IMAGEGRID RADIOLOGY VIEWER SYSTEM IG-LT1-R2H-DR-SAAS-X, IMAGEGRID RADIOLOGY VIEWER SYSTEM IG-LT1-R1H-3DV and IMAGEGRID RADIOLOGY VIEWER SYSTEM IG-5H-3DV.