Biologics Regulatory Stimlabs® LLC Announces Launch of Allacor P™ – The first FDA 510(k) cleared human umbilical cord particulate device for wound management byTim AllenJanuary 5, 2026
Spine Top Stories Spinal Simplicity Announces FDA Clearance of Minuteman® G6 MIS Fusion Device byTim AllenDecember 16, 2025
Extremities Regulatory Inside information: Bioretec has been granted FDA Breakthrough Device Designation status for its RemeOs™ DrillPin byTim AllenDecember 15, 2025
Biologics Regulatory Rapid Nexus Becomes the First Company to Receive FDA Clearance for its Advanced Wound-Healing Device Hemastyl byWill SandbergNovember 13, 2025
Financial Spine $10.75+ Bn Spinal Fusion Devices Market Insights, Competitive Landscape, and Forecasts, 2032 – Rising Incidences, Trauma from Road Accidents, and an Increase in Chronic Pain byJosh SandbergOctober 22, 2025
Extremities Top Stories Spartan Medical Inc. and Reign Medical LLC. Announce Strategic Partnership byNoah SimmonsOctober 15, 2025
Regulatory FluidAI Medical’s Origin™ device has received FDA 510(k) clearance, a pivotal milestone redefining the future of data-driven, post-operative care byNoah SimmonsSeptember 26, 2025
Regulatory Envoy Medical Advances Commercialization Planning for Breakthrough Hearing Device as FDA Clinical Trial Remains On Track byWill SandbergSeptember 26, 2025
Regulatory US opens investigation into medical equipment, device imports byWill SandbergSeptember 25, 2025
