Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Kaz USA, Inc (A Subsidiaryof Kaz 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) |
|---|---|---|---|---|---|
| K134043 | NO TOUCH+FOREHEAD NTF 3000 THERMOMETER | Kaz USA, Inc (A Subsidiaryof Kaz Inc) | 2014-05-21 | 141 | 0 |
| K103800 | BRAUN THERMOSCAN PRO 4000 SERIES AND BRAUN THERMOSCAN IRT 40 | Kaz USA, Inc (A Subsidiaryof Kaz Inc) | 2011-01-26 | 29 | 0 |
| K101747 | BRAUN THERMOSCAN PRO 4000 SERIES AND BRAUN THERMOSCAN IRT 40 | Kaz USA, Inc (A Subsidiaryof Kaz Inc) | 2010-08-04 | 43 | 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