Reflow Medical, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
Total Devices8
Categories1
Latest FDA decision2025-08-22
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251277 | CoraForce Microcatheter, CoraFlex Microcatheter | DQY | 2025-08-22 | View |
| 510(k) | K233350 | SINC Support Catheter | DQY | 2024-02-08 | View |
| 510(k) | K201811 | coraForce and coraFlex Support Catheters | DQY | 2020-10-26 | View |
| 510(k) | K190393 | Wingman 14C Crossing Catheter | DQY | 2019-05-09 | View |
| 510(k) | K173661 | Wingman 35 Crossing Catheter | DQY | 2018-04-18 | View |
| 510(k) | K173662 | speX Support Catheter | DQY | 2017-12-20 | View |
| 510(k) | K170996 | Wingman 14C Crossing Catheter | DQY | 2017-06-09 | View |
| 510(k) | K160848 | Wingman 18 Crossing Catheter | DQY | 2016-07-14 | View |
No matching devices.
Related Clinical Trials
NCT03807531A Study of the Temporary Spur Stent for the Treatment of Narrowing and Blockages in the Arteries Below the KneeACTIVE_NOT_RECRUITINGNCT05358353A Prospective Single-Arm Multicenter StuDy of the BarE TEmporary SPur StEnt System foR the tREatment of Vascular Lesions Located in the infrapoplitEal Arteries beLow the Knee (DEEPER REVEAL)COMPLETEDNCT06117150Pilot Study of the Coronary Spur Stent for In-stent Restenosis (DEEPER CORONARY)COMPLETED