Toro Neurovascular, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3031311812
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Toro 88 Superbore Catheter Ref K252297
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3031311812
- Address
- 470 Wald, Irvine, CA, 92618
Frequently asked questions
How many devices does TORO NEUROVASCULAR, INC. have in the registry?
The registry currently lists 4 devices for TORO NEUROVASCULAR, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list TORO NEUROVASCULAR, INC.'s devices?
Among its 4 most recently registered devices, TORO NEUROVASCULAR, INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do TORO NEUROVASCULAR, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for TORO NEUROVASCULAR, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TORO NEUROVASCULAR, INC. in the registry?
The most recently registered devices listed for TORO NEUROVASCULAR, INC. include Toro 88 Superbore Catheter AX088110, Toro 88 Superbore Catheter AX088110S, Toro 88 Superbore Catheter AX088118 and Toro 88 Superbore Catheter.