Dirotian Pty., Ltd.
AustraliaFDA applicant, unverified
- Devices
- 1
What Dirotian Pty., Ltd. makes
Dirotian Pty. , Ltd. makes the DENE BRIDGE device.
The DENE BRIDGE is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dene Bridge Ref K903672
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dirotian Pty., Ltd. have in the registry?
The registry currently lists 1 device for Dirotian Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dirotian Pty., Ltd.'s devices?
Among its 1 most recently registered device, Dirotian Pty., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dirotian Pty., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dirotian Pty., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dirotian Pty., Ltd. in the registry?
The most recently registered devices listed for Dirotian Pty., Ltd. include DENE BRIDGE.