Riverpoint Medical is one of 12929 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Riverpoint Medical - FDA 510(k) Cleared Devices
Recent clearances: Iconix Knotless T, ProZip Knotless Implant, HS Fiber
28
Total
28
Cleared
0
Denied
Riverpoint Medical has 28 FDA 510(k) cleared medical devices. Based in Portland, US.
Latest FDA clearance: Aug 2026. Active since 2009. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Riverpoint Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Riverpoint Medical
28 devices
Cleared
Aug 27, 2026
Iconix Knotless T
Orthopedic
28d
Cleared
Oct 16, 2025
ProZip Knotless Implant
General & Plastic Surgery
27d
Cleared
Aug 13, 2025
HS Fiber
General & Plastic Surgery
30d
Cleared
Jul 30, 2025
Iconix Speed Anchor
Orthopedic
22d
Cleared
Nov 19, 2024
Iconix Knotless Anchor
Orthopedic
27d
Cleared
Oct 29, 2024
OC JuggerKnotless Soft Anchor
Orthopedic
28d
Cleared
Aug 19, 2024
RibFix Titan™ Fixation System
Orthopedic
104d
Cleared
Jul 03, 2024
Iconix® Anchor
Orthopedic
30d
Cleared
Apr 11, 2024
OC JuggerKnot Soft Anchor
Orthopedic
27d
Cleared
Feb 23, 2024
Iconix Knotless Anchor
Orthopedic
29d
Cleared
Feb 21, 2024
ProCinch, QuadCinch
Orthopedic
28d
Cleared
Jan 05, 2024
HS Fiber Sutures
General & Plastic Surgery
256d