Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Bison Medical Co, Ltd. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K161670 | Lucid Q-PTP / HWA 55 | Bison Medical Co, Ltd. | 2016-11-02 | 139 | 0 |
| K160227 | ACCENTO / HWA Dual/Single laser | Bison Medical Co, Ltd. | 2016-04-22 | 84 | 0 |
| K150997 | RUBY STAR | Bison Medical Co, Ltd. | 2015-12-22 | 251 | 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