Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Verily Life Sciences, LLC — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K242508 | Verily Numetric Retinal Camera | Verily Life Sciences, LLC | 2024-12-09 | 109 | 0 |
| K213357 | Study Watch with Irregular Pulse Monitor (Home), Study Watch | Verily Life Sciences, LLC | 2022-07-19 | 280 | 0 |
| K192415 | Study Watch with Irregular Pulse Monitor | Verily Life Sciences, LLC | 2020-01-17 | 135 | 0 |
| K182456 | Study Watch | Verily Life Sciences, LLC | 2019-01-17 | 132 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda