FDA applicant

Mittler Supply, Inc.

South Bend, IN2 decisions1996–19960 recalls

FDA records 2 decisions for Mittler Supply, Inc. (South Bend, IN) in 1996: 2 510(k) clearances. All are in product code BXK (Gas, Calibration (Specified Concentration)). 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 Mittler Supply, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mittler Supply, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mittler Supply, Inc.

Which product codes does it file in?

What has FDA decided for it lately?