510(k) Report

FDA applicant

Dyn-A-Med Products

Mchenry, IL5 decisions1980–19840 recalls

FDA records 5 decisions for Dyn-A-Med Products (Mchenry, IL) from 1980 to 1984: 5 510(k) clearances. Most are in product codes HHT (Spatula, Cervical, Cytological) and DRX (Electrode, Electrocardiograph). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Dyn-A-Med Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dyn-A-Med Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dyn-A-Med Products 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?

  • HHTSpatula, Cervical, Cytological1decision
  • DRXElectrode, Electrocardiograph1decision
  • KGXTape And Bandage, Adhesive1decision
  • FKKClamp, Line1decision

What has FDA decided for it lately?

  • K844121Clamp, Tubing, LineDyn-A-Med Products · 1984
  • K813176Gel ElectrodeDyn-A-Med Products · 1981
  • K811157Blade, TongueDyn-A-Med Products · 1981
  • K802764Plastic Adhesive BandageDyn-A-Med Products · 1980
  • K802139Spatula, Cervical Cytological CytologyDyn-A-Med Products · 1980

All 5 as Dyn-A-Med Products →