Medical Device Manufacturer · US , Portland , OR

Riverpoint Medical, LLC - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2020

Recent clearances: Fast Absorbing PGLA, Strut Suture, LigaMend

View 12 510(k) Devices ↓

Total

Cleared

Denied

Riverpoint Medical, LLC has 12 FDA 510(k) cleared orthopedic devices. Based in Portland, US.

Latest FDA clearance: Sep 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.

Riverpoint Medical, LLC is one of 26090 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Riverpoint Medical, LLC

12 devices

1-12 of 12

Cleared Sep 29, 2026

Fast Absorbing PGLA

K263073 · GAM

General & Plastic Surgery · 28d

OsseoFit Interfacing Anchor

K242494 · MBI

Orthopedic · 96d

Cleared Oct 06, 2023

JuggerKnot Soft Anchor OC

Knotless Suture Anchor

JuggerKnot Soft Anchor

General & Plastic Surgery · 31d

Riverpoint Medical, LLC - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Riverpoint Medical, LLC

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