510(k) Report

FDA applicant

The Torrent Corp.

Mchenry, IL3 decisions1977–19840 recalls

FDA records 3 decisions for The Torrent Corp. (Mchenry, IL) from 1977 to 1984: 3 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and FMA (Depressor, Tongue, Non-Surgical). 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 and plastic surgery panel, where it files most

How often FDA has decided The Torrent Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Torrent Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Torrent Corp. 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?

  • KKXDrape, Surgical, Antimicrobial1decision
  • FMADepressor, Tongue, Non-Surgical1decision
  • NABGauze / Sponge,Nonresorbable For External Use1decision

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.

  • K842461Tongue DepressorThe Torrent Corp. · 19841cites it

What has FDA decided for it lately?

  • K842461Tongue DepressorThe Torrent Corp. · 1984
  • K780394Gauze FluffThe Torrent Corp. · 1978
  • K770621Stockinette, SurgicalThe Torrent Corp. · 1977

All 3 as The Torrent Corp. →