Denterprise International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Denterprise International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: QuickRayPRO, MobileX Portable X-ray System
4
Total
4
Cleared
0
Denied
Denterprise International, Inc. has 4 FDA 510(k) cleared medical devices. Based in Ormond Beach, US.
Last cleared in 2023. Active since 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Denterprise International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by 510k FDA Consulting / Denterprise International, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Denterprise International, Inc.
4 devices