Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sedecal USA, 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) |
|---|---|---|---|---|---|
| K042361 | DIGITAL PORTABLE X-RAY UNITS, MODEL SP-HF-4.0 D | Sedecal USA, Inc. | 2004-09-29 | 29 | 0 |
| K012546 | OPTIMA URS UNIVERSAL RADIOGRAPHIC SYSTEM | Sedecal USA, Inc. | 2001-11-02 | 87 | 2 |
| K012663 | EASY MOVING MOBILE X-RAY UNIT (MODEL SM-HF) | Sedecal USA, Inc. | 2001-08-31 | 18 | 1 |
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