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FDA 510(k)

LANDR Contact LENS Case

K-Number: K252175 · 2026-02-10

ApplicantFourth Axis, LLC
Decision Date2026-02-10
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LANDR Contact LENS Case is a medical device manufactured by Fourth Axis, LLC. It received FDA 510(k) clearance on 2026-02-10 under approval number K252175. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANDR Contact LENS Case?

LANDR Contact LENS Case is a medical device that received FDA 510(k) clearance on 2026-02-10. It is manufactured by Fourth Axis, LLC. The 510(k) number is K252175.

When was LANDR Contact LENS Case approved by the FDA?

LANDR Contact LENS Case received FDA 510(k) clearance on 2026-02-10, under approval number K252175.

What company makes LANDR Contact LENS Case?

LANDR Contact LENS Case is manufactured by Fourth Axis, LLC.

What is the FDA product code for LANDR Contact LENS Case?

The FDA product code for LANDR Contact LENS Case is LRX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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