FDA applicant
Changsha Anxiang Medical Technology Co., Ltd.
FDA records 8 decisions for Changsha Anxiang Medical Technology Co., Ltd. (Changsha, CN) from 2024 to 2025: 8 510(k) clearances. Most are in product codes NGX (Stimulator, Muscle, Powered, For Muscle…) and NUH (Stimulator, Nerve, Transcutaneous…). Since 2016 its 510(k)s took a median of 93 days from receipt to decision, against 93 for FDA’s reviews in the same codes and years. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Changsha Anxiang Medical Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
6in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Changsha Anxiang Medical 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) ReportOther applicant names beginning “Changsha”
FDA records each applicant name separately; these may or may not be the same firm.