Cultiv8 1, LLC
Country not established FDA FEI 3045178474
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Cultiv8 1, LLC makes
Cultiv8 1, LLC manufactures the Genie MAX Large Bore Introducer Sheath. This device is designed for use as an introducer sheath.
The company is based in the United States. Its product portfolio is regulated as Class II medical devices and is listed in the FDA 510(k) registry.
Catalogue
- GUDID
Genie MAX Large Bore Introducer Sheath Ref K253652
510(k) 510(k)
Company details
- FDA FEI number
- 3045178474
- DUNS number
- 125894973
- Address
- 3405 Annapolis Ln N Ste 200, Minneapolis, MN, 55447
Frequently asked questions
How many devices does Cultiv8 1, LLC have in the registry?
The registry currently lists 2 devices for Cultiv8 1, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cultiv8 1, LLC's devices?
Among its 2 most recently registered devices, Cultiv8 1, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cultiv8 1, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cultiv8 1, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cultiv8 1, LLC in the registry?
The most recently registered devices listed for Cultiv8 1, LLC include Genie MAX MAX1833 and Genie MAX Large Bore Introducer Sheath.