Data / Medical devices / United States / Fourth Axis LLC
Fourth Axis LLC: FDA-registered device maker in Boise, ID, United States, 1 510(k) clearance
Fourth Axis LLC is registered with the FDA (registration 3046398174) in Boise, ID, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 10, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3046398174
- Address
- 8139 S Eyele Ave, Boise, ID, United States, 83716
- Owner or operator
- Fourth Axis LLC (10095987)
- Roles
- Specification developer
- First device listed
- June 3, 2026
- Registered through
- 2026
- Brand names listed
- LANDR, LANDR Contact LENS Case
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Case, Contact Lens | LRX | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 10, 2026 | K252175 | LANDR Contact LENS Case | LRX | Substantially Equivalent | Fourth Axis, LLC | accessdata.fda.gov |
Compare with other makers
Updated February 10, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.