Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dentalmax 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) |
|---|---|---|---|---|---|
| K241151 | LUXEN 5G | Dentalmax Co., Ltd. | 2024-09-30 | 158 | 0 |
| K212548 | LUXEN CL Dental Liquid | Dentalmax Co., Ltd. | 2021-12-06 | 115 | 0 |
| K171585 | LUXEN Zr, LUXEN Smile | Dentalmax Co., Ltd. | 2018-10-31 | 518 | 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