Intervention Tech, Inc. ; dba Corvention
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- Devices
- 12
What Intervention Tech, Inc. ; dba Corvention makes
Intervention Tech, Inc. manufactures the KardiaPSI Balloon Catheter, a device designed for coronary interventions to facilitate angioplasty procedures by improving blood flow in blocked arteries.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Search and filter all 12 devicesCompany details
- DUNS number
- 144872016
Frequently asked questions
How many devices does Intervention Tech, Inc. ; dba Corvention have in the registry?
The registry currently lists 12 devices for Intervention Tech, Inc. ; dba Corvention. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intervention Tech, Inc. ; dba Corvention's devices?
Among its 12 most recently registered devices, Intervention Tech, Inc. ; dba Corvention has devices listed in FDA 510(k) (1 device) and FDA GUDID (11 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Intervention Tech, Inc. ; dba Corvention's devices fall under?
Among its 12 most recently registered devices, the classes recorded for Intervention Tech, Inc. ; dba Corvention's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intervention Tech, Inc. ; dba Corvention in the registry?
The most recently registered devices listed for Intervention Tech, Inc. ; dba Corvention include KardiaPSI CVPSI1925, KardiaPSI CVPSI2025, KardiaPSI CVPSI2125 and KardiaPSI CVPSI2225.