510(k) Report

FDA applicant

Ahlstrom Dexter

Windsor Locks, CT3 decisions1980–19940 recalls

FDA records 3 decisions for Ahlstrom Dexter (Windsor Locks, CT) from 1980 to 1994: 3 510(k) clearances. All are in product code FRG (Wrap, Sterilization). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Ahlstrom Dexter since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ahlstrom Dexter 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?

  • FRGWrap, Sterilization3decisions

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.

  • K800123Dextex II Sterilization WrapAhlstrom Dexter · 19801cites it

What has FDA decided for it lately?

  • K933550Hydraspun M Sterilization WrapAhlstrom Dexter · 1994
  • K893764Sterilization Tray LinerAhlstrom Dexter · 1989
  • K800123Dextex II Sterilization WrapAhlstrom Dexter · 1980

All 3 as Ahlstrom Dexter →

Other applicant names beginning “Ahlstrom”

FDA records each applicant name separately; these may or may not be the same firm.

Ahlstrom Nonwovens, LLC 2Ahlstrom Mount Holly Springs, LLC 1Ahlstrom-Munksjo Nonwovens, LLC 1