510(k) Report

FDA applicant

Vesta, Inc.

Mchenry, IL4 decisions1979–19830 recalls

FDA records 4 decisions for Vesta, Inc. (Mchenry, IL) from 1979 to 1983: 4 510(k) clearances. Most are in product codes BTQ (Airway, Nasopharyngeal) and KOD (Catheter, Urological). No recall is linked to its devices.

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

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

How often FDA has decided Vesta, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vesta, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vesta, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • BTQAirway, Nasopharyngeal3decisions
  • KODCatheter, Urological1decision

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.

  • K792018Silicone Rubber-BI Nasopharyngeal AirVesta, Inc. · 19791cites it

What has FDA decided for it lately?

  • K834078Silicone Rugger Disposable Yoke-CpapVesta, Inc. · 1983
  • K810960Nasopharyngeal AirwayVesta, Inc. · 1981
  • K7927193 Way Urethral Irrigation CatheterVesta, Inc. · 1980
  • K792018Silicone Rubber-BI Nasopharyngeal AirVesta, Inc. · 1979

All 4 as Vesta, Inc. →