Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
B&W Tek, Inc. · Predicate Candidate Screening
1 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K062363 | BWF-5 MEDICAL LASER SERIES, 810 NM; 930 NM; 980 NM; 1080 NM | B&W Tek, Inc. | 2007-01-17 | 160 | 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