510(k) Report

FDA applicant

Dispos-A-Scope

Lewiston, ID1 decision2000–20000 recalls

FDA records 1 decision for Dispos-A-Scope (Lewiston, ID) in 2000: 1 510(k) clearance. All are in product code FER (Anoscope And Accessories). 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 Dispos-A-Scope’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dispos-A-Scope since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dispos-A-Scope 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?

  • FERAnoscope And Accessories1decision

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.

  • K993738Dispos-a-ScopeDispos-A-Scope · 20001cites it

What has FDA decided for it lately?

  • K993738Dispos-a-ScopeDispos-A-Scope · 2000

The one decision as Dispos-A-Scope →