FDA applicant

Cher Mel Corp.

Mchenry, IL7 decisions1984–19860 recalls

FDA records 7 decisions for Cher Mel Corp. (Mchenry, IL) from 1984 to 1986: 7 510(k) clearances. Most are in product codes LDE (Stethoscope, Manual) and GFI (Osteotome, Manual). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Cher Mel Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cher Mel Corp.

Which product codes does it file in?

What has FDA decided for it lately?