Uramix, Inc.
Country not established FDA FEI 3001642379
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Uramix, Inc. makes
Uramix, Inc. manufactures the CuraWay Biopsy Needle, a device designed for tissue sampling in medical procedures.
The CuraWay Biopsy Needle is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Uramix CuraWay Biopsy Needle Ref K203141
510(k) 510(k)
Company details
- FDA FEI number
- 3001642379
- Address
- 272 N. LANSDOWNE AVE., E Lansdowne, PA, 19050
Frequently asked questions
How many devices does Uramix, Inc. have in the registry?
The registry currently lists 1 device for Uramix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uramix, Inc.'s devices?
Among its 1 most recently registered device, Uramix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Uramix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Uramix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Uramix, Inc. in the registry?
The most recently registered devices listed for Uramix, Inc. include Uramix CuraWay Biopsy Needle.