FDA applicant

Cybernet Medical

Ann Arbor, MI1 decision2003–20034 recalls

FDA records 1 decision for Cybernet Medical (Ann Arbor, MI) in 2003: 1 510(k) clearance. All are in product code DXH (Transmitters And Receivers…). Its devices cite 3 predicates, 0 of them its own earlier devices. 4 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Cybernet Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cybernet Medical since 2007.

Recalls per year

4in 2008

2007high 4 (2008) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Cybernet Medical’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 “Cybernet”

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

Cybernet Systems Co., Ltd. 1

Cybernet Medical

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?

What has been recalled?

Other applicant names beginning “Cybernet”