# MY01, Inc.

- Location (FDA's records): Montreal, CA
- FDA decisions: 6 (2020–2026): 6 510(k) clearances
- Product codes: LXC (6)
- Predicates its devices cite: 6 (5 its own); citations of its devices by later devices: 6 (5 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Twin Star Medical, Inc.: 1 (https://510kreport.com/company/twin-star-medical)

## Firms that cite its devices most
- Compremium AG: 1 (https://510kreport.com/company/compremium)

## Its most-cited devices
- K210525: MY01 Continuous Compartmental Pressure Monitor (2021), cited by 2
- K242997: MY01 Continuous Compartmental Pressure Monitor (2025), cited by 1
- K193321: MY01 Continuous Compartmental Pressure Monitor (2020), cited by 1
- K202635: MY01 Continuous Compartmental Pressure Monitor (2020), cited by 1
- K220952: MY01 Continuous Compartmental Pressure Monitor (2022), cited by 1

## Recent decisions
- K251900: MY01 Continuous Compartmental Pressure Monitor (Jan 16, 2026)
- K242997: MY01 Continuous Compartmental Pressure Monitor (Mar 13, 2025)
- K220952: MY01 Continuous Compartmental Pressure Monitor (May 24, 2022)
- K210525: MY01 Continuous Compartmental Pressure Monitor (Apr 22, 2021)
- K202635: MY01 Continuous Compartmental Pressure Monitor (Dec 10, 2020)
- K193321: MY01 Continuous Compartmental Pressure Monitor (Jul 30, 2020)

Source page: https://510kreport.com/company/my01