510(k) Report

FDA applicant

Disco, Inc.

West Linn, OR2 decisions1991–19930 recalls

FDA records 2 decisions for Disco, Inc. (West Linn, OR) from 1991 to 1993: 2 510(k) clearances. All are in product code DXC (Clamp, Vascular). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Disco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Disco, 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?

  • DXCClamp, Vascular2decisions

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.

  • K923085Quicklamp SystemDisco, Inc. · 19931cites it

What has FDA decided for it lately?

  • K923085Quicklamp SystemDisco, Inc. · 1993
  • K914149Femoral Artery Pressure Pad/DiskDisco, Inc. · 1991

All 2 as Disco, Inc. →

Other applicant names beginning “Disco”

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

Disco-O-Tech Medical Technologies, Ltd. 9