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Bioretec wins FDA 510(k) clearance for ActivaScrew Cannulated COM compression screw

PUBT·09/05/2026 09:25:31
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Bioretec wins FDA 510(k) clearance for ActivaScrew Cannulated COM compression screw
  • Bioretec secured FDA 510(k) clearance for its ActivaScrew Cannulated COM bioabsorbable compression screw.
  • Clearance enables US commercialization for fixation procedures in upper and lower extremities in skeletally mature adults.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Bioretec Oyj published the original content used to generate this news brief via Cision (Ref. ID: 20260904:BIT:6549:0) on September 05, 2026, and is solely responsible for the information contained therein.