AgNovos Healthcare USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
AgNovos Healthcare USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: JGH1 Core Deccompression Procedure Kit, JGH1 Bone Graft Substitute
2
Total
2
Cleared
0
Denied
AgNovos Healthcare USA, LLC has 2 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by AgNovos Healthcare USA, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - AgNovos Healthcare USA, LLC
2 devices