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FDA 510(k)

LacertaMatrix

K-Number: K252673 · 2025-12-22

ApplicantLacerta Life Science
Decision Date2025-12-22
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

LacertaMatrix is a medical device manufactured by Lacerta Life Science. It received FDA 510(k) clearance on 2025-12-22 under approval number K252673. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LacertaMatrix?

LacertaMatrix is a medical device that received FDA 510(k) clearance on 2025-12-22. It is manufactured by Lacerta Life Science. The 510(k) number is K252673.

When was LacertaMatrix approved by the FDA?

LacertaMatrix received FDA 510(k) clearance on 2025-12-22, under approval number K252673.

What company makes LacertaMatrix?

LacertaMatrix is manufactured by Lacerta Life Science.

What is the FDA product code for LacertaMatrix?

The FDA product code for LacertaMatrix is KGN.

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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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