Envisioneering, LLC is one of 25138 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Envisioneering, LLC - FDA 510(k) Cleared Devices
Recent clearances: TARGETSCAN BIOPSY KIT, TARGETSCAN BIOPSY NEEDLE GUIDE, TARGETSCAN BIOPSY KIT, TARGETSCN TRANSRECTAL ULTRASOUND SYSTEM
4
Total
3
Cleared
0
Denied
Envisioneering, LLC has 3 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 3 cleared submissions from 2004 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Envisioneering, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Envisioneering, LLC
4 devices