Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Wykle Research, 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) |
|---|---|---|---|---|---|
| K952670 | CUPRALLOY | Wykle Research, Inc. | 1995-08-25 | 74 | 0 |
| K921571 | 1ST IMPRESSION | Wykle Research, Inc. | 1993-09-10 | 526 | 0 |
| K910632 | ACCU-MIX AMALGAMATOR | Wykle Research, Inc. | 1991-03-15 | 30 | 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