Maduro Medical, Inc.
Country not established FDA establishment FEI 3027319104
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
What Maduro Medical, Inc. makes
Maduro Medical, Inc. manufactures vascular access catheters and guide catheters, including the Radical 6F Access Catheter and the Radical the Dude 7F/8F Guide Catheter. These devices are designed for use in interventional radiology and cardiology procedures, facilitating vascular access and guiding other catheters within blood vessels.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are intended for use in the United States.
Catalogue
Radical 064 Reperfusion Catheter Ref K261089
510(k) 510(k)Radical 6F Access Catheter Ref K253975
510(k) 510(k)Radical the Dude 7F Guide Catheter Ref K231393
510(k) 510(k)Radical the Dude 8F Guide Catheter Ref K243577
510(k) 510(k)
Company details
- FDA FEI number
- 3027319104
- Address
- 983 University Ave Bldg A, Los Gatos, CA, 95032
Frequently asked questions
How many devices does MADURO MEDICAL, INC. have in the registry?
The registry currently lists 4 devices for MADURO MEDICAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MADURO MEDICAL, INC.'s devices?
Among its 4 most recently registered devices, MADURO MEDICAL, INC. has devices listed in FDA 510(k) (4 devices).
What risk classes do MADURO MEDICAL, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for MADURO MEDICAL, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MADURO MEDICAL, INC. in the registry?
The most recently registered devices listed for MADURO MEDICAL, INC. include Radical 064 Reperfusion Catheter, Radical 6F Access Catheter, Radical the Dude 7F Guide Catheter and Radical the Dude 8F Guide Catheter.