Titan Technology Intl., Inc.
Country not established
- Devices
- 1
What Titan Technology Intl., Inc. makes
Titan Technology Intl., Inc. manufactures the TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE, a medical device designed for patient transport between hospital segments or departments, facilitating safe movement while maintaining patient stability and comfort.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Titan Meridian Intersegmental Rollertable Ref K905756
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Titan Technology Intl., Inc. have in the registry?
The registry currently lists 1 device for Titan Technology Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Titan Technology Intl., Inc.'s devices?
Among its 1 most recently registered device, Titan Technology Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Titan Technology Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Titan Technology Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Titan Technology Intl., Inc. in the registry?
The most recently registered devices listed for Titan Technology Intl., Inc. include TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE.