510(k) Report

FDA applicant

Tadco, Inc.

Stamford, CT2 decisions1991–19930 recalls

FDA records 2 decisions for Tadco, Inc. (Stamford, CT) from 1991 to 1993: 2 510(k) clearances. Most are in product codes CCW (Laryngoscope, Rigid) and KMK (Device, Intravascular Catheter Securement). 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 Tadco, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tadco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tadco, 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?

  • CCWLaryngoscope, Rigid1decision
  • KMKDevice, Intravascular Catheter Securement1decision

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.

  • K926158Slater SleeveTadco, Inc. · 19931cites it

What has FDA decided for it lately?

  • K926158Slater SleeveTadco, Inc. · 1993
  • K905735Genny Denny IV ShieldTadco, Inc. · 1991

All 2 as Tadco, Inc. →