# Saneso, Inc.

- Location (FDA's records): Pittsburgh, PA
- FDA decisions: 2 (2022–2023): 2 510(k) clearances
- Product codes: OCX (1), FDF (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)

## Its most-cited devices
- K210052: 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)) (2022), cited by 1

## Recent decisions
- K222173: Saneso Lens Wash Bottle Assembly (SAN-LWB-A) (Feb 27, 2023)
- K210052: 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)) (Apr 1, 2022)

Source page: https://510kreport.com/company/saneso