Cionic, Inc.
United StatesFDA applicant, unverified
Cionic, Inc. is a medical device manufacturer, with 9 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 9
Registry facts
- Registries
- FDA GUDID 6
- FDA 510(k) 3
- Device classes
- FDA Class II 9
- Identifiers
- DUNS 081351601
Catalogue
- Regimes: 510(k) Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Cionic Neural Sleeve NS-100 Ref K221823
Regimes: 510(k) Registry: 510(k)Cionic Neural Sleeve NS-100 Ref K213622
Regimes: 510(k) Registry: 510(k)Cionic Neural Sleeve (Ns-200) Ref K243828
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 081351601
- support@cionic.com
- Phone
- 8884813724
Frequently asked questions
How many devices does Cionic, Inc. have in the registry?
The registry currently lists 9 devices for Cionic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cionic, Inc.'s devices?
Among its 9 most recently registered devices, Cionic, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cionic, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Cionic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cionic, Inc. in the registry?
The most recently registered devices listed for Cionic, Inc. include CIONIC NS-200, CIONIC DC-100, CIONIC NS-100 and CIONIC SL-100.