Nextgen Biologics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nextgen Biologics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeoMatriX Wound Matrix, NeoMatriX Wound Matrix
2
Total
2
Cleared
0
Denied
Nextgen Biologics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Gainesville, US.
Last cleared in 2021. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Nextgen Biologics, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and Hogan Lovells Llp.
FDA 510(k) Regulatory Record - Nextgen Biologics, Inc.
2 devices