- 1 ORTHOFIX: Announces FDA Approval of STIM onTrack 2.1 Mobile App for Bone Growth Stimulators
- 2 CARELIGHT: Introduces Line Of FDA-Cleared Light Therapy Devices; Recognized Industry Leader Joins Sales Team
- 3 SOLITON: Files Special 510(k) with FDA for its Generation II RAP Device
- 4 HYPERFINE: World’s First Bedside MRI System Receives FDA 510(k) Clearance
- 5 BLUEGRASS VASCULAR TECHNOLOGIES: FDA Grants De Novo Clearance to Bluegrass Vascular Technologies for the Surfacer® Inside-Out® Access Catheter System
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