Celestray Biotech Company, LLC., is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Celestray Biotech Company, LLC., - FDA 510(k) Cleared Devices
Recent clearances: Rebuilder Nerve Guidance Conduit, SpinMedix Absorbable Fibrous Membrane
2
Total
2
Cleared
0
Denied
Celestray Biotech Company, LLC., has 2 FDA 510(k) cleared medical devices. Based in Bethesda, US.
Latest FDA clearance: Jan 2024. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Celestray Biotech Company, LLC., Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Celestray Biotech Company, LLC.,
2 devices