Renovorx, Inc.
United StatesFDA applicant, unverified FDA FEI 3011279674
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA FEI, FDA recalls
Catalogue
RenovoCath Ref K191606
Regimes: 510(k) Registry: 510(k)RenovoCath Ref K160067
Regimes: 510(k) Registry: 510(k)Renovocath RC120 Ref K141175
Regimes: 510(k) Registry: 510(k)RenovoCath Ref K212324
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011279674
- DUNS number
- 057757944
- Address
- 2570 W El Camino, Mountain View, CA, 94040
- [email protected]
- Phone
- 16502844433
FDA recalls
2015
- 25 Nov 2015 Z-0565-2016 Class II Terminated Incorrect version of Instructions for Use were shipped to two US customers.
Frequently asked questions
How many devices does Renovorx, Inc. have in the registry?
The registry currently lists 4 devices for Renovorx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Renovorx, Inc.'s devices?
Among its 4 most recently registered devices, Renovorx, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Renovorx, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Renovorx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Renovorx, Inc.?
FDA recall records list 1 recall initiated by Renovorx, Inc., the most recent initiated on 25 Nov 2015. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Renovorx, Inc. in the registry?
The most recently registered devices listed for Renovorx, Inc. include RenovoCath and RENOVOCATH RC120.