Mobileodt, Ltd.
IsraelFDA applicant, unverified
Mobileodt, Ltd. is a medical device manufacturer, with 4 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 15 Nov 2026.
- Devices
- 4
Registry facts
- Registries
- FDA GUDID 3
- FDA 510(k) 1
- Device classes
- FDA Class II 4
- Identifiers
- DUNS 600049276
What Mobileodt, Ltd. makes
Mobileodt, Ltd. manufactures the EVA (Enhanced Visual Assessment) System, a colposcope designed for cervical lesion detection and assessment in clinical settings.
The EVA System is classified as a Class II medical device and is listed under FDA’s 510(k) and UDI registries.
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
EVA (Enhanced Visual Assessment) System Ref K161871
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 600049276
Frequently asked questions
How many devices does Mobileodt, Ltd. have in the registry?
The registry currently lists 4 devices for Mobileodt, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mobileodt, Ltd.'s devices?
Among its 4 most recently registered devices, Mobileodt, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Mobileodt, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Mobileodt, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mobileodt, Ltd. in the registry?
The most recently registered devices listed for Mobileodt, Ltd. include EVA System 2, EVA System 3.0, EVA System EVA 3 Plus/EVA 3.1 and EVA (Enhanced Visual Assessment) System.