Mali-Tech, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Mali-Tech, Ltd. makes
Mali-Tech, Ltd. manufactures the Goldfinger Device, a Class II medical device designed for specific diagnostic or procedural applications in radiology or interventional medicine.
The company’s portfolio is regulated under FDA 510(k) clearance requirements, with the Goldfinger Device listed in the U.S. regulatory system. Mali-Tech, Ltd. is based in the United States.
Catalogue
Goldfinger Device Ref K001162
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mali-Tech, Ltd. have in the registry?
The registry currently lists 1 device for Mali-Tech, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mali-Tech, Ltd.'s devices?
Among its 1 most recently registered device, Mali-Tech, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mali-Tech, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mali-Tech, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mali-Tech, Ltd. in the registry?
The most recently registered devices listed for Mali-Tech, Ltd. include GOLDFINGER DEVICE.