Fourth Axis, LLC
Country not established FDA FEI 3046398174
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Fourth Axis, LLC makes
Fourth Axis, LLC manufactures the LANDR Contact Lens Case, a reusable storage container designed for holding and cleaning single-use contact lenses.
The LANDR Contact Lens Case is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- GUDID
LANDR Contact LENS Case Ref K252175
510(k) 510(k)
Company details
- FDA FEI number
- 3046398174
- DUNS number
- 121335018
- Address
- 8139 S Eyele Ave, Boise, ID, 83716
- [email protected]
- Phone
- 8053051793
Frequently asked questions
How many devices does Fourth Axis, LLC have in the registry?
The registry currently lists 2 devices for Fourth Axis, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fourth Axis, LLC's devices?
Among its 2 most recently registered devices, Fourth Axis, 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 Fourth Axis, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fourth Axis, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fourth Axis, LLC in the registry?
The most recently registered devices listed for Fourth Axis, LLC include LANDR LANDR_SAGE_001 and LANDR Contact LENS Case.