Wallaby Medical
Wallaby Medical appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 18, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K254071 | p17 XR Microcatheter | August 18, 2026 |
| K240917 | Esperance 3+ Aspiration Catheter System | October 1, 2024 |
| K231056 | Esperance Distal Access Catheter | March 8, 2024 |
| K232437 | Paragon 8F Balloon Guide Catheter | October 13, 2023 |
| K223139 | Wallaby 017 Micro Catheter | April 25, 2023 |
| K222603 | 6F Wallaby Long Sheath | March 2, 2023 |
| K211697 | Esperance Aspiration Catheter System | November 16, 2021 |
| K173711 | Wallaby Avenir Coil System | May 4, 2018 |