Carecubes, Inc.
United Statesfrom the FDA registration address FDA FEI 3038166862
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Carecubes, Inc. makes
Carecubes, Inc. manufactures the Carecube Negative Pressure Isolation Chamber, a device designed for isolating patients to contain airborne pathogens and reduce infection risk in healthcare settings.
The company’s product portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Search and filter all 11 devicesCompany details
- FDA FEI number
- 3038166862
- DUNS number
- 117860649
- Address
- 4440 Round Lake Rd W, Arden Hills, MN, 55112
- [email protected]
- Phone
- 2027432273
Frequently asked questions
How many devices does Carecubes, Inc. have in the registry?
The registry currently lists 11 devices for Carecubes, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carecubes, Inc.'s devices?
Among its 11 most recently registered devices, Carecubes, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (9 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Carecubes, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Carecubes, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Carecubes, Inc. in the registry?
The most recently registered devices listed for Carecubes, Inc. include Carecube Negative Pressure Isolation Chamber (1BY), Carecube ISTARI 1BX-991-00036, Carecube ISTARI 1BX-610-00101 and Carecube ISTARI 1BX-930-00008.