510(k) Report

FDA applicant

Chongqing Moffy Innovation Technology Co., Ltd.

Chongqing, CN2 decisions2024–20240 recalls

FDA records 2 decisions for Chongqing Moffy Innovation Technology Co., Ltd. (Chongqing, CN) in 2024: 2 510(k) clearances. Most are in product codes BZH (Meter, Peak Flow, Spirometry) and BYI (Percussor, Powered-Electric). 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 Chongqing Moffy Innovation Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2024

2024: 2
2024high 2 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Chongqing Moffy Innovation Technology Co., Ltd. by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Other applicant names beginning “Chongqing”

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