Instanosis, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Instanosis, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InstaStrip Fentanyl Rapid Test (Urine)
1
Total
1
Cleared
0
Denied
Instanosis, Inc. has 1 FDA 510(k) cleared medical devices. Based in King Of Prussia, US.
Latest FDA clearance: Mar 2024. Active since 2024. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Instanosis, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LSI International, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Instanosis, Inc.
1 devices