Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Innomed Corp. · 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) |
|---|---|---|---|---|---|
| K872747 | LASER CENTERING DEVICE | Innomed Corp. | 1987-09-04 | 53 | 0 |
| K822574 | INNOMED PD-1 KIT | Innomed Corp. | 1982-10-13 | 50 | 0 |
| K827796 | INNOSCAN EXAMINATION LIGHT | Innomed Corp. | 1982-08-24 | 26 | 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