Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Innova Life Sciences Corp. · 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) |
|---|---|---|---|---|---|
| K052951 | ENDOPORE ANATOMIC ENDOSSEOUS DENTAL IMPLANT SYSTEM | Innova Life Sciences Corp. | 2006-01-27 | 99 | 0 |
| K053242 | PITT-EASY DENTAL IMPLANT SYSTEM | Innova Life Sciences Corp. | 2006-01-06 | 49 | 0 |
| K043190 | SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM | Innova Life Sciences Corp. | 2004-12-14 | 27 | 0 |
| K032140 | 5.0 X 5MM ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM | Innova Life Sciences Corp. | 2003-10-02 | 83 | 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