Riverpoint Medical, LLC - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Riverpoint Medical, LLC has 11 FDA 510(k) cleared orthopedic devices. Based in Portland, US.
Latest FDA clearance: Mar 2026. Active since 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Riverpoint Medical, LLC
11 devices
Cleared
Mar 11, 2026
Strut Suture
Orthopedic
110d
Cleared
Feb 27, 2026
LigaMend
Orthopedic
98d
Cleared
Mar 20, 2025
RootMend MRR
Orthopedic
84d
Cleared
Nov 26, 2024
OsseoFit Interfacing Anchor
Orthopedic
96d
Cleared
Oct 06, 2023
JuggerKnot Soft Anchor OC
Orthopedic
57d
Cleared
Oct 05, 2023
All-Suture Anchor
Orthopedic
171d
Cleared
Aug 01, 2023
Knotless Suture Anchor
Orthopedic
90d
Cleared
Jul 26, 2023
HS Fiber Cerclage
Orthopedic
497d
Cleared
May 17, 2023
JuggerKnot Soft Anchor
Orthopedic
27d
Cleared
Feb 23, 2023
OrthoButton AL
Orthopedic
28d
Cleared
Sep 10, 2020
HS Fiber
General & Plastic Surgery
31d