510(k) Report

FDA applicant

Wuhu Snnda Medical Treatment Appliance Technology

Shanghai, CN1 decision2013–20130 recalls

FDA records 1 decision for Wuhu Snnda Medical Treatment Appliance Technology (Shanghai, CN) in 2013: 1 510(k) clearance. All are in product code HFX (Clamp, Circumcision). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Wuhu Snnda Medical Treatment Appliance Technology’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013: 1
2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Wuhu Snnda Medical Treatment Appliance Technology by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wuhu Snnda Medical Treatment Appliance…’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 “Wuhu”

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