FDA applicant

Litton Systems, Inc.

Davenport, IA4 decisions1987–20020 recalls

FDA records 4 decisions for Litton Systems, Inc. (Davenport, IA) from 1987 to 2002: 4 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and 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, anesthesiology panel, where it files most

How often FDA has decided Litton Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Litton Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Litton”

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

Litton Medical Electronics 38 Litton Bionetics 15 Litton Dental Products 12 Litton Medical Systems 8 Litton Datamedix 5

Litton Systems, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Litton”