510(k) Report

FDA applicant

American Medical Development, Inc.

Boston, MA1 decision1993–19930 recalls

FDA records 1 decision for American Medical Development, Inc. (Boston, MA) in 1993: 1 510(k) clearance. All are in product code CCX (Support, Patient Position). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for American Medical Development, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — American Medical Development, 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?

  • CCXSupport, Patient Position1decision

What has FDA decided for it lately?

  • K934235Sniff Position PillowAmerican Medical Development, Inc. · 1993

The one decision as American Medical Development, Inc. →