Bend IT Technologies, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K252213 | Bendit17 Microcatheter | December 3, 2025 |
| K203842 | Bendit21 Microcatheter | April 13, 2022 |
| K200582 | Bendit2.7 Steerable Microcatheter | June 25, 2020 |
| K190126 | Bendit2.7 Steerable Microcatheter | August 22, 2019 |