Changsha Anxiang Medical Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251429 | OTC 4-Channel Rechargeable TENS Unit | August 28, 2025 |
| K251706 | TENS and EMS Unit | July 30, 2025 |
| K251187 | 3 in 1 TENS UNIT (TC1241, TC2241, TS1241) | July 28, 2025 |
| K250759 | 3 in 1 TENS UNIT | June 13, 2025 |
| K243763 | Wireless TENS & EMS Unit | March 12, 2025 |
| K243511 | OTC TENS & EMS Unit | February 10, 2025 |
| K242787 | Tens & Ems Device (TU1080) | December 18, 2024 |
| K242567 | Muscle and Nerve Stimulator TENS & EMS (TP2208), Muscle and Nerve Stimulator TENS & EMS (TP2208C) | November 4, 2024 |