FDA applicant

Nexsys Electronics

San Leandro, CA2 decisions1995–20060 recalls

FDA records 2 decisions for Nexsys Electronics (San Leandro, CA) from 1995 to 2006: 2 510(k) clearances. Most are in product codes LMD (System, Digital Image Communications…) and LLZ (System, Image Processing, Radiological). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Nexsys Electronics, Inc.”.

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 Nexsys Electronics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nexsys Electronics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nexsys Electronics’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Nexsys”

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

Nexsys Electronics Inc. Dba Medweb 1

Nexsys Electronics

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Nexsys”