Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account
Dyna Flex — 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) |
|---|---|---|---|---|---|
| K230225 | DynaFlex Clear Brackets & Buttons | Dyna Flex | 2023-06-05 | 129 | 0 |
| K190583 | DynaFlex | Dyna Flex | 2019-06-27 | 113 | 0 |
| K121396 | DYNAFLEX | Dyna Flex | 2012-08-14 | 97 | 0 |
| K103076 | DYNAFLEX | Dyna Flex | 2011-02-23 | 128 | 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