Trilogic Corp.
Country not established
- Devices
- 1
What Trilogic Corp. makes
Trilogic Corp. manufactures the WHISPER O2, a medical device designed for oxygen delivery in clinical settings, likely targeting precise and low-noise ventilation support for patients.
The WHISPER O2 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Whisper O2 Ref K931355
510(k) 510(k)
Frequently asked questions
How many devices does Trilogic Corp. have in the registry?
The registry currently lists 1 device for Trilogic Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trilogic Corp.'s devices?
Among its 1 most recently registered device, Trilogic Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Trilogic Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Trilogic Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trilogic Corp. in the registry?
The most recently registered devices listed for Trilogic Corp. include WHISPER O2.