Moximed, Inc.
FDA Regulatory Profile
Moximed, Inc. appears in FDA public data with 1 recall, 1 510(k) clearance, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0762-2025, Class II) was initiated on December 2, 2024. Its most recent 510(k) clearance was granted on April 10, 2023.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 2
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-0762-2025 | Class II | MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: | December 2, 2024 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| DEN220033 | MISHA Knee System | April 10, 2023 |