Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Whip Mix Corporation · 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) |
|---|---|---|---|---|---|
| K241729 | Hard Splint & Thermo-Adaptive Splint | Whip Mix Corporation | 2025-03-18 | 277 | 0 |
| K190107 | VeriSplint | Whip Mix Corporation | 2019-07-10 | 169 | 0 |
| K152443 | Vericore Gradient Temporary Disc | Whip Mix Corporation | 2016-05-11 | 258 | 0 |
| K142670 | Vericore Zirconia Blanks | Whip Mix Corporation | 2014-10-22 | 33 | 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