Renovorx Inc

FDA Filings

This page includes the latest FDA filings for Renovorx Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3011279674
FEI Number3011279674
NameRENOVORX, INC.
Owner & OperatorRenovoRx, Inc.
Contact Address4546 El Camino Real Suite 223
Los Altos CA 94022 US
Official Correspondent
  • Debra Cogan
  • 1-408-5150820-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4546 El Camino Real Ste 223
Los Altos, CA 94022 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198

FDA Filings

Device
Company
DeviceDate
Renovorx, Inc.
 RenovoCath MMRC120-DB-11112021-10-29
RenovoRx, Inc.
RenovoCath2019-08-07
RenovoRx, Inc.
RenovoCath2017-03-07
RENOVORX, INC.
RenovoCath RC120 catheter2014-11-11
RENOVORX, INC.
RENOVOCATH RC1202014-10-24

Related Finance Registrations
CAGE Code66BA1RENOVORX, INC. R & D
DUNS033461994RENOVORX, INC.
SEC0001574094RenovoRx, Inc. of DELAWARE
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