# Endophys, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 3 (2015–2016): 3 510(k) clearances
- Product codes: DYB (2), DSK (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 4 (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
- Acist Medical Systems, Inc.: 2 (https://510kreport.com/company/acist-medical-systems)
- Togo Medikit Co., Ltd.: 1 (https://510kreport.com/company/togo-medikit)
- Endologix, Inc.: 1 (https://510kreport.com/company/endologix)
- Millar Instruments, Inc.: 1 (https://510kreport.com/company/millar-instruments)
- Radi Medical Systems AB: 1 (https://510kreport.com/company/radi-medical-systems)

## Firms that cite its devices most
- Endophys Holdings, LLC: 3 (https://510kreport.com/company/endophys-holdings)

## Its most-cited devices
- K160272: Endophys Pressure Sensing Sheath Kit (2016), cited by 2
- K141275: Endophys Pressure Sensing Sheath Kit (2015), cited by 1
- K141615: Endophys Blood Pressure Monitor (2015), cited by 1

## Recent decisions
- K160272: Endophys Pressure Sensing Sheath Kit (Mar 4, 2016)
- K141275: Endophys Pressure Sensing Sheath Kit (Jan 7, 2015)
- K141615: Endophys Blood Pressure Monitor (Jan 7, 2015)

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