Truvic Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Truvic Medical, Inc. makes
Truvic Medical, Inc. manufactures thrombectomy systems, including the Symphony and Prodigy devices, designed for the mechanical removal of blood clots in vascular procedures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Symphony Thrombectomy System Ref K223216
Regimes: 510(k) Registry: 510(k)Prodigy Thrombectomy System Ref K214114
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Truvic Medical, Inc. have in the registry?
The registry currently lists 2 devices for Truvic Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Truvic Medical, Inc.'s devices?
Among its 2 most recently registered devices, Truvic Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Truvic Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Truvic Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Truvic Medical, Inc. in the registry?
The most recently registered devices listed for Truvic Medical, Inc. include Symphony Thrombectomy System and Prodigy Thrombectomy System.