FDA applicant

Survival Technology, Inc.

Bethesda, MD10 decisions1977–19930 recalls

FDA records 10 decisions for Survival Technology, Inc. (Bethesda, MD) from 1977 to 1993: 10 510(k) clearances. Most are in product codes DXH (Transmitters And Receivers…) and FMF (Syringe, Piston). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Survival Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Survival Technology, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?