Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sunpex Technology Co., 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) |
|---|---|---|---|---|---|
| K033019 | SUNPEX TECHNOLOGIES MODEL SE03 | Sunpex Technology Co., Ltd. | 2004-01-22 | 118 | 0 |
| K024175 | SUNPEX TECHNOLOGIES MODEL PW | Sunpex Technology Co., Ltd. | 2003-05-01 | 134 | 0 |
| K021925 | SUNPEX TECHNOLOGIES MODEL SE 01 | Sunpex Technology Co., Ltd. | 2002-11-08 | 150 | 0 |
| K021371 | SUNSPEX TECHNOLOGIES MODEL SE 02 | Sunpex Technology Co., Ltd. | 2002-05-16 | 16 | 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