# Changsha Anxiang Medical Technology Co., Ltd.

- Location (FDA's records): Changsha, CN
- FDA decisions: 8 (2024–2025): 8 510(k) clearances
- Product codes: NGX (5), NUH (3)
- 510(k) review time since 2016: median 93 days, against 93 for FDA's reviews in the same codes and years (7 of 8 faster)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K251429: OTC 4-Channel Rechargeable TENS Unit (Aug 28, 2025)
- K251706: TENS and EMS Unit (Jul 30, 2025)
- K251187: 3 in 1 TENS UNIT (TC1241, TC2241, TS1241) (Jul 28, 2025)
- K250759: 3 in 1 TENS UNIT (Jun 13, 2025)
- K243763: Wireless TENS & EMS Unit (Mar 12, 2025)
- K243511: OTC TENS & EMS Unit (Feb 10, 2025)
- K242787: Tens & Ems Device (TU1080) (Dec 18, 2024)
- K242567: Muscle and Nerve Stimulator TENS & EMS (TP2208), Muscle and Nerve Stimulator TENS & EMS (TP2208C) (Nov 4, 2024)

Source page: https://510kreport.com/company/changsha-anxiang-medical-technology