Intervene Inc
United Statesfrom the FDA registration address FDA establishment FEI 3030481118
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Stratus Infusion Catheter Ref K222185
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3030481118
- Address
- 2684 Middlefield Rd Ste E, Redwood City, CA, 94063
Frequently asked questions
How many devices does INTERVENE INC have in the registry?
The registry currently lists 9 devices for INTERVENE INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list INTERVENE INC's devices?
Among its 9 most recently registered devices, INTERVENE INC has devices listed in FDA 510(k) (2 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do INTERVENE INC's devices fall under?
Among its 9 most recently registered devices, the classes recorded for INTERVENE INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from INTERVENE INC in the registry?
The most recently registered devices listed for INTERVENE INC include Recana Debulking Catheter FG014, Recana Introducer Sheath, 13Fr x 30cm FG017, Recana Collection Basket, 30mm FG016 and Recana Collection Basket, 18mm FG015.