FDAnews
www.fdanews.com/articles/178385-ossix-volumax-receives-fda-510k-clearance

Ossix Volumax Receives FDA 510(k) Clearance

September 12, 2016

Datum Dental’s Ossix Volumax dental regenerative has received FDA 510(k) clearance.

This product is designed to restore lost volume in guided bone regeneration (GBR), guided tissue regeneration (GTR) and soft tissue augmentation cases.

This device is currently available in the U.S. and is currently available in four sizes, ranging from 10 x 12.5 mm to 30 x 40 mm. — Cynthia Jessup

View today's stories