Elminda, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Elminda, Ltd. makes
Elminda, Ltd. manufactures the BNA Platform, a device designed for bronchoscopic navigation and biopsy, aiding in precise lung tissue sampling and diagnostic procedures.
The BNA Platform is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
BNA Platform Ref K202588
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elminda, Ltd. have in the registry?
The registry currently lists 1 device for Elminda, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elminda, Ltd.'s devices?
Among its 1 most recently registered device, Elminda, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Elminda, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Elminda, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elminda, Ltd. in the registry?
The most recently registered devices listed for Elminda, Ltd. include BNA Platform.