FDA applicant

Aspect Electronics, Inc.

San Leandro, CA3 decisions1995–19960 recalls

FDA records 3 decisions for Aspect Electronics, Inc. (San Leandro, CA) from 1995 to 1996: 3 510(k) clearances. Most are in product codes LMC (Camera, Multi Format, Radiological) and LMA (Digitizer, Image, 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 Aspect Electronics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aspect Electronics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Aspect Electronics, 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 “Aspect”

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

Aspect Medical Systems, Inc. 25 Aspect Imaging, Ltd. 6 Aspect Vision Care, Ltd. 5

Aspect Electronics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Aspect”