FDA applicant

Servox Medizintechnik GmbH

Koln, DE1 decision2002–20020 recalls

FDA records 1 decision for Servox Medizintechnik GmbH (Koln, DE) in 2002: 1 510(k) clearance. All are in product code BTA (Pump, Portable, Aspiration (Manual Or Powered)). 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 Servox Medizintechnik GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Servox Medizintechnik GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Servox Medizintechnik GmbH

Which product codes does it file in?

What has FDA decided for it lately?