510(k) Report

FDA applicant

Centurion Medical Products Corporation

Williamston, MI3 decisions2011–20221 recall

FDA records 3 decisions for Centurion Medical Products Corporation (Williamston, MI) from 2011 to 2022: 3 510(k) clearances. Most are in product codes DRS (Transducer, Blood-Pressure, Extravascular) and DQX (Wire, Guide, Catheter). Its devices cite 4 predicates, 0 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “Centurion Medical Products”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Centurion Medical Products Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2011: 12016: 12022: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Centurion Medical Products Corporation by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DRSTransducer, Blood-Pressure, Extravascular1decision
  • DQXWire, Guide, Catheter1decision
  • FPASet, Administration, Intravascular1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K103562Centurion Pressure Injectable Extension SetCenturion Medical Products Corporation · 20111cites it

What has FDA decided for it lately?

  • K210548Medline Integrated Arterial CatheterCenturion Medical Products · 2022
  • K161408Compass Cast and MAPCenturion Medical Products Corporation · 2016
  • K103562Centurion Pressure Injectable Extension SetCenturion Medical Products Corporation · 20111 recall

All 2 as Centurion Medical Products Corporation →The one decision as Centurion Medical Products →

What has been recalled?

1 recall linked to its devices; the latest:

  • K030099Ultra-Filtration (UF) Removal Regulators (Rgltr Assy UF REM Molded Spare); a spare part…Jun 21, 2006