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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 the device name listed in this FDA 510(k) record. The listed applicant is Fourth Axis, LLC. It received FDA 510(k) clearance on 2026-02-10 under 510(k) 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. The listed applicant is Fourth Axis, LLC. The 510(k) number is K252175.

When did LANDR Contact LENS Case receive FDA 510(k) clearance?

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

Who is the listed applicant for LANDR Contact LENS Case?

The FDA 510(k) record lists Fourth Axis, LLC as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: LRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas LimitedK173365Bausch + Lomb Boston Scleral Lens CaseBausch & Lomb, Incorporated

Official Source

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

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