Illuminoss Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Illuminoss Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IlluminOss Photodynamic Bone Stabilization System, IlluminOss Bone Stabilization System, IlluminOss Photodynamic Bone Stabilization System
Illuminoss Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in East Providence, US.
Latest FDA clearance: Jan 2024. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Illuminoss Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC, Musculoskeletal Clinical Regulatory Affairs and Musculoskeltal Clinical Regulatory Advisers, LLC. 1 device has linked clinical trial registered on ClinicalTrials.gov.