510(k) Report

FDA applicant

Redfield Corp.

Washington, D.C., DC1 decision1991–19910 recalls

FDA records 1 decision for Redfield Corp. (Washington, D.C., DC) in 1991: 1 510(k) clearance. All are in product code KNS (Unit, Electrosurgical, Endoscopic (With Or…). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Redfield Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Redfield 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?

  • KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K911648Redfield Infrared CoagulatorRedfield Corp. · 19912cite it

What has FDA decided for it lately?

  • K911648Redfield Infrared CoagulatorRedfield Corp. · 1991

The one decision as Redfield Corp. →