Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Alcon, Inc. — 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) |
|---|---|---|---|---|---|
| K071236 | ALCON MULTI-PURPOSE SOLUTION | Alcon, Inc. | 2007-12-12 | 223 | 0 |
| K040231 | INTELIPORT OCCLUDING DEVICE | Alcon, Inc. | 2004-07-13 | 162 | 0 |
| K031193 | SOFT (HYDROPHILIC) CONTACT LENS CARE SOLUTION | Alcon, Inc. | 2003-07-03 | 78 | 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