Saneso, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Saneso, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Saneso Lens Wash Bottle Assembly (SAN-LWB-A), Saneso Colonoscope 360-A (Model: with/without Select Band Imaging (SBI) and with/without Dual Band Imaging(DBI)), Saneso Single Camera Colonoscope-A (Model: with/without Select Band Imaging (SBI)), Saneso Gastroscope 360-A (Model: with/without Select Band Imaging (SBI) and with/without Dual Band Imaging(DBI)), Saneso Single Camera Gastroscope-A (Model: with/without Select Band Imaging (SBI))
2
Total
2
Cleared
0
Denied
Saneso, Inc. has 2 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Last cleared in 2023. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Saneso, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Elexes Medical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Saneso, Inc.
2 devices