Genesee Biomedical, Inc.
Genesee Biomedical, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2026, with 1 FDA device recall on record.
Top product codes for Genesee Biomedical, Inc.
FDA recalls by Genesee Biomedical, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Genesee Biomedical, Inc.
- K252917 — ATLAAS (Atraumatic Left Atrial Appendage System) (AD)
- K250859 — TransForm McCarthy Mitral Annuloplasty Ring (TF)
- K232599 — TransForm McCarthy Mitral Annuloplasty Ring (TF)
- K230679 — WellsForm Tricuspid Annuloplasty Band (WF)
- K202253 — TruForm Sievers Annuloplasty Ring
- K190506 — NeoForm Annuloplasty Ring
- K161815 — FlexForm Annuloplasty Ring and FlexForm Annuloplasty Band
- K093903 — ATS TRI-AD SEMI-FLEXIBLE TRICUSPID ANUULOPLASTY, MODEL 900SFC
- K090428 — ATS SIMULUS ADJUSTABLE FLEXIBLE ANNULOPLASTY, MODEL 735 AC
- K083683 — ATS SIMULUS SEMI-RIGID MITRAL ANNULOPLASTY RING, MODEL 800SC
- K072655 — ATS SIMULUS SEMI-RIGID MITRAL ANNULOPLASTY RING, MODEL 800SR
- K071214 — ATS SIMULUS ADJUSTABLE FLEXIBLE ANNULOPLASTY RING
- K052565 — ATS SIMULUS ANNULOPLASTY RING, MODEL 700FF
- K052899 — ATS SIMULUS ANNULOPLASTY BAND, MODEL 700FC
Data sourced from openFDA. This site is unofficial and independent of the FDA.