FDA 510(k)

LANDR Contact LENS Case

K-번호: K252175 · 2026-02-10

결정일2026-02-10

제품 코드LRX

자문 위원회OP

결정Substantially Equivalent

기기 요약

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.

자주 묻는 질문

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.

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LANDR Contact LENS Case

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: LRX)

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