510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K250859Substantially Equivalent

TransForm McCarthy Mitral Annuloplasty Ring (TF)

Genesee BioMedical, Inc., Denver CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K250859 is the FDA 510(k) clearance record for TransForm McCarthy Mitral Annuloplasty Ring (TF), a class II device, cleared for Genesee Biomedical, Inc. on under FDA product code KRH (Ring, Annuloplasty). FDA records list 14 510(k) clearances for Genesee Biomedical, Inc., from to . As of , FDA records show no recalls naming K250859.

Clearance record

Decision date
Received
(126 days to decision)
Product code
KRH Ring, Annuloplasty
Regulation
21 CFR 870.3800
Device class
Class II
Review panel
Cardiovascular
Applicant
Genesee Biomedical, Inc. 700 W. Mississippi Ave., Unit D-5, Denver CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KRH

Trailing 12 months
2 clearances under product code KRH in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KRH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260