Brief: Bioretec Receives FDA 510(K) Clearance For Its Activascrew Cannulated Com Bioabsorbable Compression Screw
05/09/2026 10:26
BRIEF-Bioretec Receives FDA 510(K) Clearance For Its Activascrew Cannulated Com Bioabsorbable Compression Screw Sept 5 (Reuters) - Bioretec Oy BRETEC.HE:
BIORETEC RECEIVES FDA 510(K) CLEARANCE FOR ITS ACTIVASCREW™ CANNULATED COM BIOABSORBABLE COMPRESSION SCREW
Source text: ID:nWkr6KxQL4
Further company coverage: BRETEC.HE
((Reuters.Briefs@thomsonreuters.com;))
Recent news on Bioretec Oy
See all newsBrief: Bioretec Initiates Change Negotiations
Brief: Bioretec Gets Marketing Authorization From FDA
Brief: Bioretec Receives FDA 510(K) Clearance For Its Activascrew Cannulated Com Bioabsorbable Compression Screw
Finland's Bioretec H1 revenue rises 12%, loss narrows
Brief: Bioretec Q2 Net Sales EUR 1.1 Million