Elfi-Tech, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Elfi-Tech, Ltd. makes
Elfi-Tech, Ltd. manufactures the Elfor-L, a medical device designed for [specific application not provided in data]. This product falls under specialized diagnostic or therapeutic use, though precise details on its function are not specified in the provided information.
The Elfor-L is classified as a Class II device under regulatory frameworks, requiring premarket notification (510(k)) clearance through the FDA. The company is based in the United States, and its device portfolio is listed in the FDA’s 510(k) registry.
Catalogue
Elfor-L Ref K243852
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elfi-Tech, Ltd. have in the registry?
The registry currently lists 1 device for Elfi-Tech, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elfi-Tech, Ltd.'s devices?
Among its 1 most recently registered device, Elfi-Tech, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Elfi-Tech, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Elfi-Tech, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elfi-Tech, Ltd. in the registry?
The most recently registered devices listed for Elfi-Tech, Ltd. include Elfor-L.