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FDA 510(k)

LYMA Laser PRO

K-Number: K243330 · 2025-02-21

ApplicantLyma Life , Ltd.
Decision Date2025-02-21
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LYMA Laser PRO is a medical device manufactured by Lyma Life , Ltd.. It received FDA 510(k) clearance on 2025-02-21 under approval number K243330. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYMA Laser PRO?

LYMA Laser PRO is a medical device that received FDA 510(k) clearance on 2025-02-21. It is manufactured by Lyma Life , Ltd.. The 510(k) number is K243330.

When was LYMA Laser PRO approved by the FDA?

LYMA Laser PRO received FDA 510(k) clearance on 2025-02-21, under approval number K243330.

What company makes LYMA Laser PRO?

LYMA Laser PRO is manufactured by Lyma Life , Ltd..

What is the FDA product code for LYMA Laser PRO?

The FDA product code for LYMA Laser PRO is OHS.

Other Devices by Lyma Life , Ltd.

K210823LYMA Laser

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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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