FDA applicant

Taga Medical Technologies, Inc.

Eastlake, OH3 decisions2001–20040 recalls

FDA records 3 decisions for Taga Medical Technologies, Inc. (Eastlake, OH) from 2001 to 2004: 3 510(k) clearances. All are in product code BTT (Humidifier, Respiratory Gas, (Direct Patient…). Its devices cite 4 predicates, 2 of them its own earlier devices. 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 Taga Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Taga Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Taga Medical Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?