510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K221520Substantially Equivalent

Miro3D Wound Matrix

Reprise Biomedical, Inc., Plymouth MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221520 is the FDA 510(k) clearance record for Miro3D Wound Matrix, cleared for Reprise Biomedical, Inc. on under FDA product code KGN (Wound Dressing With Animal-Derived Material(S)). FDA records list 5 510(k) clearances for Reprise Biomedical, Inc., from to . As of , FDA records show no recalls naming K221520.

Clearance record

Decision date
Received
(85 days to decision)
Product code
KGN Wound Dressing With Animal-Derived Material(S)
Device class
Unclassified
Review panel
Unknown
Applicant
Reprise Biomedical, Inc. 17400 Medina Rd., Plymouth MN
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