Innoblative Designs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Innoblative Designs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SIRA™ RFA Electrosurgical Device, SIRA RFA Electrosurgical Device
2
Total
2
Cleared
0
Denied
Innoblative Designs, Inc. has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.
Last cleared in 2023. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Innoblative Designs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Innoblative Designs, Inc.
2 devices