MicroPort NeuroTech (Shanghai) Co., Ltd.
MicroPort NeuroTech (Shanghai) Co., Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 20, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K260351 | Numen Helia Coil Embolization System; NumenFR Detachment System | May 20, 2026 |
| K242154 | Numen Coil Embolization System; NumenFR Detachment System | September 30, 2024 |
| K232955 | Numen Coil Embolization System; NumenFR Detachment System | January 10, 2024 |
| K203625 | Numen Coil Embolization System; NumenFR Detachment System | September 1, 2021 |