FDA applicant

Metronic Electronic GmbH

Hampton, VA1 decision1993–19930 recalls

FDA records 1 decision for Metronic Electronic GmbH (Hampton, VA) in 1993: 1 510(k) clearance. All are in product code LDD (Dc-Defibrillator, Low-Energy, (Including…). 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 Metronic Electronic GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Metronic Electronic GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Metronic”

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

Metronic, Inc. 4

Metronic Electronic GmbH

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Metronic”