Genesis Biosystems, Inc. is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genesis Biosystems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LipiVage, GENESIS LED WANDS, ACCELAWAVE SYSTEM
4
Total
4
Cleared
0
Denied
Genesis Biosystems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Lewisville, US.
Historical record: 4 cleared submissions from 2008 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Genesis Biosystems, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Emergo Global Consulting, LLC.
FDA 510(k) Regulatory Record - Genesis Biosystems, Inc.
4 devices