FDA applicant

Stihler Electronic, C/O Worldwide Regul. Services

Farmingville, NY1 decision1988–19880 recalls

FDA records 1 decision for Stihler Electronic, C/O Worldwide Regul. Services (Farmingville, NY) in 1988: 1 510(k) clearance. All are in product code LGZ (Warmer, Thermal, Infusion Fluid). 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 hospital panel, where it files most

How often FDA has decided Stihler Electronic, C/O Worldwide Regul. Services’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stihler Electronic, C/O Worldwide Regul. Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Stihler Electronic, C/O Worldwide Regul. Services by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Stihler”

FDA records each applicant name separately; these may or may not be the same firm.

Stihler Electronic GmbH 7

Stihler Electronic, C/O Worldwide Regul. Services

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Stihler”