Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Cantor & Silver , Ltd. · 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) |
|---|---|---|---|---|---|
| K994320 | CHROMAGEN V2.0 HAPLOSCOPIC SYSTEM & COLOR VISION ENHANCEMENT | Cantor & Silver , Ltd. | 2000-10-20 | 303 | 0 |
| K992500 | CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DA | Cantor & Silver , Ltd. | 1999-08-18 | 23 | 0 |
| K990757 | CANTOR & SILVER 5X TINTED (HIOXIFILCON A) SOFT (SPHERICAL & | Cantor & Silver , Ltd. | 1999-04-21 | 44 | 0 |
| K981779 | CANTOR & SILVER 5X (HIOXIFILCON A) SOFT (SPHERICAL & TORIC) | Cantor & Silver , Ltd. | 1998-06-24 | 35 | 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