Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Anker Innovations Limited · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K254300 | eufy Wearable Breast Pump (T600P, T6000, T6001, T6002, T6003 | Anker Innovations Limited | 2026-05-29 | 149 | 0 |
| K250207 | eufy Wearable Breast Pump S1 (T8D02); eufy Wearable Breast P | Anker Innovations Limited | 2025-08-11 | 199 | 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