Hd Lifesciences, LLC is one of 18972 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hd Lifesciences, LLC - FDA 510(k) Cleared Devices
Recent clearances: Hive™ Stand-alone Anterior Lumbar Interbody System, HD LifeSciences Cervical IBFD System, HD Lumbar Interbody System
3
Total
3
Cleared
0
Denied
Hd Lifesciences, LLC has 3 FDA 510(k) cleared medical devices. Based in Stoneham, US.
Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hd Lifesciences, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Hd Lifesciences, LLC
3 devices