Ultrathera Technologies, Inc.
Country not established FDA establishment FEI 3027406982
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Ultrathera Technologies, Inc. makes
Ultrathera Technologies, Inc. manufactures the GyroStim medical device.
The GyroStim is classified as a Class U device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
GyroStim Ref K220231
510(k) 510(k)
Company details
- FDA FEI number
- 3027406982
- Address
- 2 N Cascade Avenue, Colorado Springs, CO, 80903
Frequently asked questions
How many devices does ULTRATHERA TECHNOLOGIES, INC. have in the registry?
The registry currently lists 1 device for ULTRATHERA TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ULTRATHERA TECHNOLOGIES, INC.'s devices?
Among its 1 most recently registered device, ULTRATHERA TECHNOLOGIES, INC. has devices listed in FDA 510(k) (1 device).
What are the newest devices from ULTRATHERA TECHNOLOGIES, INC. in the registry?
The most recently registered devices listed for ULTRATHERA TECHNOLOGIES, INC. include GyroStim.