Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Wide Corporation — Predicate Candidate Screening
20 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
54 daysmedian FDA review time
243 days90th percentile
20clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K222719 | CX50N | Wide Corporation | 2023-05-09 | 243 | 0 |
| K222716 | MX50N | Wide Corporation | 2023-05-08 | 242 | 0 |
| K222722 | CW60N | Wide Corporation | 2022-10-31 | 53 | 0 |
| K222717 | CL24N | Wide Corporation | 2022-10-31 | 53 | 0 |
| K210493 | CX30N (CX30PQX) | Wide Corporation | 2021-04-14 | 54 | 0 |
| K210491 | CW120N | Wide Corporation | 2021-04-08 | 48 | 0 |
| K170781 | MX50N(MX50YQS) | Wide Corporation | 2017-04-04 | 20 | 0 |
| K170783 | CX50N(CX50YQS) | Wide Corporation | 2017-03-31 | 16 | 0 |
| K160354 | MX50T(MX50TQS) | Wide Corporation | 2016-05-02 | 84 | 0 |
| K160353 | MX50N(MX50YQS) | Wide Corporation | 2016-04-22 | 74 | 0 |
| K160348 | CX30N (CX30PQX) | Wide Corporation | 2016-04-14 | 66 | 0 |
| K160346 | MX30N(MX30TQS) | Wide Corporation | 2016-04-14 | 66 | 0 |
| K160351 | CX50N, CX50YQS | Wide Corporation | 2016-04-07 | 59 | 0 |
| K160355 | CX20N(CX20PUX) | Wide Corporation | 2016-04-07 | 59 | 0 |
| K110596 | MW100 (MAMMOGRAPHY) LCD MONITOR SYSTEM | Wide Corporation | 2011-11-18 | 261 | 0 |
| K052312 | WIDE 5MP (MAMMO) LCD MONITOR SYSTEM | Wide Corporation | 2005-10-07 | 44 | 0 |
| K042634 | WIDE 1MP LCD MONITOR SYSTEM | Wide Corporation | 2004-10-08 | 11 | 0 |
| K032960 | WIDE 2MP TFT LCD MONITOR SYSTEM IF 1902A | Wide Corporation | 2003-10-08 | 15 | 0 |
| K032174 | WIDE 3MP GRAYSCALE TFT LCD MONITOR IF2103A | Wide Corporation | 2003-07-24 | 8 | 0 |
| K031929 | 5MP TFT LCD MONITOR SYSTEM IF2105A BY WIDE CORPORATION | Wide Corporation | 2003-07-08 | 15 | 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