Lifevac, LLC
United Statesfrom the FDA registration address FDA FEI 3011053282
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
LifeVac Ref DEN250012
Regimes: De Novo Registry: De Novo
Company details
- FDA FEI number
- 3011053282
- Address
- 110 Lake Ave South, Nesconset, NY, 11767
Frequently asked questions
How many devices does Lifevac, LLC have in the registry?
The registry currently lists 5 devices for Lifevac, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifevac, LLC's devices?
Among its 5 most recently registered devices, Lifevac, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Lifevac, LLC's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Lifevac, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifevac, LLC in the registry?
The most recently registered devices listed for Lifevac, LLC include LifeVac Travel KIT LVC3004, LifeVac School KIT LVC3003, LifeVac Home Kit LVC3001 and LifeVac EMS KIT LVC3002.