Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dicon, Inc. — 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) |
|---|---|---|---|---|---|
| K822580 | AUTO PERIOMETER 3000 | Dicon, Inc. | 1982-09-30 | 36 | 0 |
| K820877 | AUTOMATIC OBJECTIVE REFRACTOR 2000 | Dicon, Inc. | 1982-06-25 | 87 | 0 |
| K811347 | DICON AUTO PERIMETER 2000 | Dicon, Inc. | 1981-08-20 | 100 | 0 |
| K811346 | DICON AUTO PERIMETER 200 | Dicon, Inc. | 1981-08-20 | 100 | 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