Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LacertaMatrix

K-Number: K260218 · 2026-02-19

ApplicantLacerta Life Sciences
Decision Date2026-02-19
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

LacertaMatrix is a medical device manufactured by Lacerta Life Sciences. It received FDA 510(k) clearance on 2026-02-19 under approval number K260218. 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 2026-02-19. It is manufactured by Lacerta Life Sciences. The 510(k) number is K260218.

When was LacertaMatrix approved by the FDA?

LacertaMatrix received FDA 510(k) clearance on 2026-02-19, under approval number K260218.

What company makes LacertaMatrix?

LacertaMatrix is manufactured by Lacerta Life Sciences.

What is the FDA product code for LacertaMatrix?

The FDA product code for LacertaMatrix is KGN.

Related Devices (Code: KGN)

K160136Flowable Wound MatrixCook Biotech Incorporated K152600Collagen Dental Wound DressingsCollagen Matrix, Inc. K153754MicroMatrixAcell, Inc. K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc. K172010gel-e BandageGel-E, Inc. (Formerly Remedium Technologies, Inc.) K171842Geistlich Wound MatrixGeistlich Pharma AG

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.

↑