Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Propel Orthodontics, LLC — 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) |
|---|---|---|---|---|---|
| K183018 | VPro5 | Propel Orthodontics, LLC | 2019-11-01 | 366 | 0 |
| K172164 | PROPEL Device | Propel Orthodontics, LLC | 2018-01-17 | 183 | 0 |
| K150392 | PROPEL device | Propel Orthodontics, LLC | 2015-09-18 | 212 | 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