Riverpoint Medical, LLC
FDA 510(k) & PMA Approved Devices — 11 products
Total Devices11
Categories3
Latest Approval2026-03-11
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K253693 | Strut Suture; No-Tie Button | MBI | 2026-03-11 | View |
| 510(k) | K253695 | LigaMend | MBI | 2026-02-27 | View |
| 510(k) | K243988 | RootMend MRR | MBI | 2025-03-20 | View |
| 510(k) | K242494 | OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct | MBI | 2024-11-26 | View |
| 510(k) | K232411 | JuggerKnot Soft Anchor OC | MBI | 2023-10-06 | View |
| 510(k) | K231078 | All-Suture Anchor | MBI | 2023-10-05 | View |
| 510(k) | K231278 | Knotless Suture Anchor | MBI | 2023-08-01 | View |
| 510(k) | K220765 | HS Fiber Cerclage | JDQ | 2023-07-26 | View |
| 510(k) | K231128 | JuggerKnot Soft Anchor | MBI | 2023-05-17 | View |
| 510(k) | K230212 | OrthoButton AL | MBI | 2023-02-23 | View |
| 510(k) | K202242 | HS Fiber | GAT | 2020-09-10 | View |
No matching devices.