FDA applicant

Lifenet Health

Virginia Beach, VA3 decisions2008–20240 recalls

FDA records 3 decisions for Lifenet Health (Virginia Beach, VA) from 2008 to 2024: 3 510(k) clearances. Most are in product codes DXZ (Patch, Pledget And Intracardiac, Petp, Ptfe…) and FMF (Syringe, Piston). Its devices cite 4 predicates, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2024

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Lifenet Health by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Lifenet Health’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 “Lifenet”

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

Lifenet 1

Lifenet Health

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 “Lifenet”