GlobalData on MSN1d
MedCAD secures FDA 510(k) clearance for AccuStride foot and ankle system
The AccuStride System is intended to enhance surgical outcomes for proximal phalanx and metatarsal arthroplasty.
FDA grants 510(k) clearance for Huntleigh’s CTG Analysis
The Dawes-Redman CTG Analysis is designed to assess if a non-stress test trace meets the “criteria of normality".
Aurora Spine Announces FDA 510(k) Clearance for the AERO™ Facet Fusion System
Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV: ASG) (OTCQB: ASAPF), a leader in innovative spine and interventional pain management solutions, today announced that the U.S. Food and ...
Morningstar4d
Restore Robotics Receives FDA 510(k) Clearance for Remanufacturing Da Vinci Xi 8mm Monopolar Curved Scissors
HENDERSON, Nev., March 25, 2025 /PRNewswire/ -- Restore Robotics is pleased to announce it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for remanufacturing Da ...
Zacks Small Cap Research on MSN8d
MGRM: Monogram Receives Clearance from the FDA on its 510(k) Submission for its mBôs TKA System.
MGRM READ THE FULL MGRM RESEARCH REPORT On March 17, 2025, Monogram (NASDAQ:MGRM) announced that the FDA has granted 510(k) clearance for its Monogram mBôs TKA System. This determination means that ...
Morningstar4d
Aurora Spine Announces FDA 510(k) Clearance for the AERO™ Facet Fusion System
today announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the Company’s newest product, the AERO™ Facet Fusion System. The AERO MIS Facet Fusion System ...