FDA applicant

Nerv Technology Inc. (D.B.A.) Fluidai Medical

Kitchener, CA1 decision2025–20250 recalls

FDA records 1 decision for Nerv Technology Inc. (D.B.A.) Fluidai Medical (Kitchener, CA) in 2025: 1 510(k) clearance. All are in product code SFO (Electrode Measurement, Drain Effluent Ph). 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, clinical chemistry panel, where it files most

How often FDA has decided Nerv Technology Inc. (D.B.A.) Fluidai Medical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2025high 1 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2025.

FIG. 1 — Nerv Technology Inc. (D.B.A.) Fluidai Medical by year, 2025–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nerv Technology Inc. (D.B.A.) Fluidai…’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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Nerv Technology Inc. (D.B.A.) Fluidai Medical

Which product codes does it file in?

What has FDA decided for it lately?