Eximo Medical, Ltd.
Eximo Medical, Ltd. 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 April 10, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K260244 | Auryon Atherectomy System | April 10, 2026 |
| K241553 | Auryon Atherectomy Catheter 1.7mm; Auryon Atherectomy Catheter 1.7mm, Hydrophilic Coating | June 27, 2024 |
| K233668 | Auryon Atherectomy Catheter 1.5 mm XL, Hydrophilic Coating (EXM-4010-H000), Auryon Atherectomy Cathe | December 15, 2023 |
| K230709 | Auryon Atherectomy System | June 9, 2023 |
| K220116 | Auryon Atherectomy Catheters | September 26, 2022 |
| K221077 | Auryon Atherectomy System | June 9, 2022 |
| K202835 | Auryon Atherectomy System | December 2, 2020 |
| K181642 | B-Laser Atherectomy System | October 5, 2018 |