Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Angelus Industria DE Productos Odontologicos · 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) |
|---|---|---|---|---|---|
| K151047 | MTA Repair HP | Angelus Industria DE Productos Odontologicos | 2016-08-31 | 499 | 0 |
| K123823 | INTERLIG | Angelus Industria DE Productos Odontologicos | 2013-05-31 | 170 | 0 |
| K112046 | MTA ANGELUS | Angelus Industria DE Productos Odontologicos | 2012-01-06 | 172 | 0 |
| K082180 | PERMA FIBER,MODEL 441; PERMA MESH, MODEL 440 | Angelus Industria DE Productos Odontologicos | 2008-12-17 | 138 | 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