Intera Oncology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intera Oncology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Intera Refill Kit, Intera Non-coring (Huber) Refill Needles, Intera Non-coring (Huber) Special bolus Needles and OR Prep Kit
2
Total
2
Cleared
0
Denied
Intera Oncology, Inc. has 2 FDA 510(k) cleared medical devices. Based in Wellesley, US.
Last cleared in 2022. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Intera Oncology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Intera Oncology, Inc.
2 devices