510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K260218Substantially Equivalent

LacertaMatrix

Lacerta Life Sciences, Woodstock GA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K260218 is the FDA 510(k) clearance record for LacertaMatrix, cleared for Lacerta Life Sciences on under FDA product code KGN (Wound Dressing With Animal-Derived Material(S)). FDA records list one 510(k) clearance for Lacerta Life Sciences. As of , FDA records show no recalls naming K260218.

Clearance record

Decision date
Received
(27 days to decision)
Product code
KGN Wound Dressing With Animal-Derived Material(S)
Device class
Unclassified
Review panel
Unknown
Applicant
Lacerta Life Sciences 7842 Hickory Flat Hwy., Woodstock GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KGN

Trailing 12 months
16 clearances under product code KGN in the twelve months to October 2026, June 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code KGN, trailing twelve months
MonthClearances
November 20250
December 20253
January 20261
February 20262
March 20261
April 20260
May 20261
June 20265
July 20261
August 20261
September 20261
October 20260