Icentia Inc
Country not established FDA FEI 3014271754
Icentia Inc is a medical device manufacturer, with 8 devices listed in FDA GUDID (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 8
- Device classes
- FDA Class II 7
- FDA Class I 1
- Identifiers
- FDA FEI 3014271754
- DUNS 241983607
At a glance
Market reach
- United States
- FDA establishment
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
Company details
- FDA FEI number
- 3014271754
- DUNS number
- 241983607
- Address
- 2750 rue Einstein, Quebec
- Website
- www.icentia.com
- info@icentia.com
FDA establishments
- Icentia LLC Burlington, VT · US FEI 3030721635
From the company website
Icentia is both a medical devices manufacturer and a service company. We provide a line of medical testing innovations for healthcare institutions.
Frequently asked questions
How many devices does Icentia Inc have in the registry?
The registry currently lists 8 devices for Icentia Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Icentia Inc's devices?
Among its 8 most recently registered devices, Icentia Inc has devices listed in FDA GUDID (8 devices).
What risk classes do Icentia Inc's devices fall under?
Among its 8 most recently registered devices, the classes recorded for Icentia Inc's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Icentia Inc in the registry?
The most recently registered devices listed for Icentia Inc include CardioSTAT 10-006, EART 10-501 and OFIX 10-002.
Which FDA establishments are linked to Icentia Inc?
1 FDA establishment is linked to Icentia Inc in the registry; they are listed on the company page.