FDA applicant

Cmed

Irvine, CA2 decisions1995–19980 recalls

FDA records 2 decisions for Cmed (Irvine, CA) from 1995 to 1998: 2 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and IXY (Holder, Radiographic Cassette, Wall-Mounted). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Cmed since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cmed by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Cmed

Which product codes does it file in?

What has FDA decided for it lately?