Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Kestrel · 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) |
|---|---|---|---|---|---|
| K901748 | KESTREL LENS CASE (208-12NT POLYSTYRENE) | Kestrel | 1990-05-31 | 44 | 0 |
| K900053 | KESTREL LENS CASE 731H-893S/P-1700-2611 | Kestrel | 1990-01-30 | 27 | 0 |
| K900054 | KESTREL LENS CASE 1543-893S/P-1700-2611 | Kestrel | 1990-01-30 | 27 | 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