FDA applicant

Leibinger F.L. Fischer

Dallas, TX1 decision1995–19950 recalls

FDA records 1 decision for Leibinger F.L. Fischer (Dallas, TX) in 1995: 1 510(k) clearance. All are in product code IYE (Accelerator, Linear, Medical). 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 Leibinger F.L. Fischer’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Leibinger F.L. Fischer since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Leibinger F.L. Fischer by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Leibinger”

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

Leibinger GmbH 4 Leibinger & Fischer, Ltd. 2

Leibinger F.L. Fischer

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Leibinger”