Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dyna-Tek Industries · 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) |
|---|---|---|---|---|---|
| K964771 | DE-TOX CONTROL 1 AND DE-TOX CONTROL 19 | Dyna-Tek Industries | 1997-02-04 | 69 | 0 |
| K904326 | DE-TOX TUBES A AND DE-TOX TUBES B | Dyna-Tek Industries | 1991-01-17 | 119 | 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