FDA applicant

Johannah Medical Services, Inc.

Mchenry, IL4 decisions1977–19800 recalls

FDA records 4 decisions for Johannah Medical Services, Inc. (Mchenry, IL) from 1977 to 1980: 4 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and FCG (Biopsy Needle). 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 Johannah Medical Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Johannah Medical Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Johannah Medical Services, Inc.

Which product codes does it file in?

What has FDA decided for it lately?