# Verily Life Sciences, LLC

- Location (FDA's records): South San Francisco, CA
- FDA decisions: 4 (2019–2024): 4 510(k) clearances
- Product codes: DXH (3), HKI (1)
- 510(k) review time since 2016: median 134 days, against 146 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 3 (2 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
- Crystalvue Medical Corporation: 1 (https://510kreport.com/company/crystalvue-medical)
- AliveCor, Inc.: 1 (https://510kreport.com/company/alivecor)
- Qompium NV: 1 (https://510kreport.com/company/qompium)

## Firms that cite its devices most
- iRhythm Technologies, Inc.: 1 (https://510kreport.com/company/irhythm-technologies)

## Its most-cited devices
- K192415: Study Watch with Irregular Pulse Monitor (2020), cited by 2
- K182456: Study Watch (2019), cited by 1

## Recent decisions
- K242508: Verily Numetric Retinal Camera (Dec 9, 2024)
- K213357: Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor (Jul 19, 2022)
- K192415: Study Watch with Irregular Pulse Monitor (Jan 17, 2020)
- K182456: Study Watch (Jan 17, 2019)

Source page: https://510kreport.com/company/verily-life-sciences