Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Alexotek Co. — 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) |
|---|---|---|---|---|---|
| K881789 | MINILINE BRACKET | Alexotek Co. | 1988-06-01 | 36 | 0 |
| K834446 | ALEXOTEK LINGUAL TUBES | Alexotek Co. | 1984-04-05 | 111 | 0 |
| K834392 | LABIAL CUSPID TUBE | Alexotek Co. | 1984-02-28 | 76 | 0 |
| K834272 | ALEXOLOK BRACKET | Alexotek Co. | 1984-02-03 | 57 | 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