Levisense Medical, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3044677502
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3044677502
- Address
- 47 Enon St. - Unit 7, Beverly, MA, 01915
Frequently asked questions
How many devices does LEVISENSE MEDICAL, INC. have in the registry?
The registry currently lists 6 devices for LEVISENSE MEDICAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LEVISENSE MEDICAL, INC.'s devices?
Among its 6 most recently registered devices, LEVISENSE MEDICAL, INC. has devices listed in FDA GUDID (6 devices).
What risk classes do LEVISENSE MEDICAL, INC.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for LEVISENSE MEDICAL, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LEVISENSE MEDICAL, INC. in the registry?
The most recently registered devices listed for LEVISENSE MEDICAL, INC. include Pro-Daptive SensorCell Flotation Surface PDA-9100-3680, Pro-Daptive SensorCell Flotation Surface PDA-9100-3684, Pro-Daptive SensorCell Flotation Surface PDA-9100-4280 and Pro-Daptive SensorCell Flotation Surface PDA-9100-4884.