Conavi Medical Inc.
Conavi Medical Inc. appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1585-2025, Class I) was initiated on March 12, 2025. Its most recent 510(k) clearance was granted on April 17, 2026.
Summary
- Total Recalls
- 1 (1 Class I)
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1585-2025 | Class I | Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: | March 12, 2025 |