FDA Conducts Routine Onsite Inspection

The U.S. Food and Drug Administration routinely inspects medical device facilities to assess quality and regulatory compliance.  The FDA has an established framework of procedures for industry oversight in effort to protect the public and the integrity of the broader healthcare system. On December 21st 2018 Fusion Orthopedics, at their...

Fusion Orthopedics Acquires OrthoNoble

FOR IMMEDIATE RELEASE: Fusion Orthopedics is pleased to announce that it has acquired San Diego, California based OrthoNoble, LLC on November 9th, 2018. OrthoNoble is a sports-medicine medical device company specializing in the development of suture anchors for surgical treatment of ligament, tendon, and soft tissue pathologies. The assets center...

DynaBridge Staple System – FDA Cleared

After years of development, Fusion Orthopedics is pleased to announce the DynaBridge System as the newest addition to their product offering. FDA 510(k) clearance was issued October 15th, 2018. The assigned FDA 510(k) # for DynaBridge is K181815. The system is indicated for fracture and osteotomy fixation and joint arthrodesis...

Fusion Orthopedics Acquires Sgarlato Med

FOR IMMEDIATE RELEASE: Fusion Orthopedics Acquires Sgarlato Med Fusion Orthopedics is pleased to announce that as of August 24th, 2018, Fusion Orthopedics has entered into an agreement to acquire Sgarlato Med.  The agreement represents another substantial milestone for Fusion, and will be a catalyst to sales growth for the company....