Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Wheel Checkers — Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K863429 | MODIFIED DEVICE FOR SELF EXAMINATION OF EYES | Wheel Checkers | 1987-01-20 | 138 | 0 |
| K843702 | APPARATUS & METHODS SELF-EXAM OF EYE | Wheel Checkers | 1985-01-03 | 104 | 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