David F. Trungale
Country not established
- Devices
- 1
What David F. Trungale makes
David F. Trungale manufactures the SI-PRO, a surgical instrument designed for orthopedic procedures, including bone cutting and shaping.
The SI-PRO is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Si-Pro Ref K904389
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does David F. Trungale have in the registry?
The registry currently lists 1 device for David F. Trungale. Devices recorded under merged duplicate company entries are counted once.
Which registries list David F. Trungale's devices?
Among its 1 most recently registered device, David F. Trungale has devices listed in FDA 510(k) (1 device).
What risk classes do David F. Trungale's devices fall under?
Among its 1 most recently registered device, the classes recorded for David F. Trungale's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from David F. Trungale in the registry?
The most recently registered devices listed for David F. Trungale include SI-PRO.