# Verathon Medical (Canada) Ulc

- Location (FDA's records): Burnaby, CA
- FDA decisions: 6 (2019–2026): 6 510(k) clearances
- Product codes: EOQ (5), FAJ (1)
- 510(k) review time since 2016: median 37 days, against 147 for FDA's reviews in the same codes and years (5 of 6 faster)
- Predicates its devices cite: 10 (8 its own); citations of its devices by later devices: 11 (8 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
- Ambu A/S: 2 (https://510kreport.com/company/ambu-a-s)

## Firms that cite its devices most
- Hunan Vathin Medical Instrument Co., Ltd.: 3 (https://510kreport.com/company/hunan-vathin-medical-instrument)

## Its most-cited devices
- K183256: GlideScope BFlex Single-Use Bronchoscope System (2019), cited by 3
- K191948: GlideScope BFlex 5.8 Single-Use Bronchoscope (2019), cited by 2
- K230948: BFlex™ 2 Slim 3.8 Single-Use Bronchoscope (2023), cited by 2
- K211947: GlideScope BFlex 2.8 Single-Use Bronchoscope (2021), cited by 2
- K193488: GlideScope BFlex 3.8 Single-Use Bronchoscope (2020), cited by 2

## Recent decisions
- K253696: CFlex Cystoscope - Standard Deflection (0570-0455); CFlex Cystoscope - Reverse Deflection (0570-0456); CystoView Monitor (0570-0465) (May 11, 2026)
- K230948: BFlex™ 2 Slim 3.8 Single-Use Bronchoscope (May 3, 2023)
- K211947: GlideScope BFlex 2.8 Single-Use Bronchoscope (Nov 3, 2021)
- K193488: GlideScope BFlex 3.8 Single-Use Bronchoscope (Jan 16, 2020)
- K191948: GlideScope BFlex 5.8 Single-Use Bronchoscope (Aug 21, 2019)
- K183256: GlideScope BFlex Single-Use Bronchoscope System (Jan 4, 2019)

Source page: https://510kreport.com/company/verathon-medical-canada-ulc