Inflammatix, Inc.
Country not established
- Devices
- 7
What Inflammatix, Inc. makes
Inflammatix, Inc. manufactures the TriVerity diagnostic device, a system designed for analyzing inflammatory biomarkers in patient samples to support clinical decision-making.
The TriVerity system is classified as a Class II medical device and is authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
TriVerity Ref K241676
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 080387361
- [email protected]
- Phone
- 18666946359
Frequently asked questions
How many devices does Inflammatix, Inc. have in the registry?
The registry currently lists 7 devices for Inflammatix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inflammatix, Inc.'s devices?
Among its 7 most recently registered devices, Inflammatix, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Inflammatix, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Inflammatix, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inflammatix, Inc. in the registry?
The most recently registered devices listed for Inflammatix, Inc. include MYRNA-1000, TRIVERITY-2000, TriVerity Level 1 Quality Control and TriVerity Level 2 Quality Control.