Medical Device Manufacturer · US , Durham , NC

Bioventus, LLC

5 submissions · 5 cleared · Since 2017

5

Total

5

Cleared

0

Denied

Bioventus, LLC has 5 FDA 510(k) cleared medical devices. Based in Durham, US.

Latest FDA clearance: Jul 2025. Active since 2017. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Bioventus, LLC Filter by specialty or product code using the sidebar.

5 devices

1–5 of 5

StimTrial Neuromodulation System

K243782 · GZF Stimulator, Peripheral Nerve, Implanted (pain Relief) · Neurology

TalisMann Neuromodulation System

K243678 · GZF Stimulator, Peripheral Nerve, Implanted (pain Relief) · Neurology

Allograft Delivery Device (OFAC-C)

K233368 · FMF Syringe, Piston · General & Plastic Surgery

SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty

K233490 · MQV Filler, Bone Void, Calcium Compound · Orthopedic

K162860 · MQV Filler, Bone Void, Calcium Compound · Orthopedic