FDA applicant

Werner Schott Elektrogerate

West Germany, DE1 decision1986–19860 recalls

FDA records 1 decision for Werner Schott Elektrogerate (West Germany, DE) in 1986: 1 510(k) clearance. All are in product code FTC (Light, Ultraviolet, Dermatological). 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 and plastic surgery panel, where it files most

How often FDA has decided Werner Schott Elektrogerate’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Werner Schott Elektrogerate since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Werner Schott Elektrogerate’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Werner”

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

Werner Eidam Medizin-Technologie GmbH 1

Werner Schott Elektrogerate

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Werner”