Ideate Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ideate Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SteroScope® Sterilization Technology System
1
Total
1
Cleared
0
Denied
Ideate Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ideate Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Corrigan Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Ideate Medical, Inc.
1 devices