FDA applicant

Kontron Elektronik GmbH

San Leandro, CA1 decision1991–19910 recalls

FDA records 1 decision for Kontron Elektronik GmbH (San Leandro, CA) in 1991: 1 510(k) clearance. All are in product code LLZ (System, Image Processing, Radiological). 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, radiology panel, where it files most

How often FDA has decided Kontron Elektronik GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kontron Elektronik GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kontron Elektronik 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 “Kontron”

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

Kontron Instruments, Inc. 58 Kontron Medical Systems Sas 4 Kontron Electronics 3 Kontron, Inc. 1

Kontron Elektronik GmbH

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kontron”