FDA applicant

Feellife Health, Inc.

Shenzhen, CN2 decisions2020–20230 recalls

FDA records 2 decisions for Feellife Health, Inc. (Shenzhen, CN) from 2020 to 2023: 2 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BZG (Spirometer, Diagnostic). 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, anesthesiology panel, where it files most

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

FDA decisions per year

1in 2023

2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Feellife Health, Inc. by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Feellife Health, Inc.

Which product codes does it file in?

What has FDA decided for it lately?