Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Whip Mix Corp. — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
149 daysmedian FDA review time
282 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K140877 | VERICORE ZIRCONIA BLANKS | Whip Mix Corp. | 2014-09-03 | 149 | 0 |
| K140146 | COMFORTSOFT SOFT DENTURE LINER SYSTEM | Whip Mix Corp. | 2014-04-29 | 97 | 0 |
| K131760 | WHIP MIX PREPPIES PLUS | Whip-Mix Corp. | 2014-03-26 | 282 | 0 |
| K092857 | VERICORE ABUTMENT IN TITANIUM FOR IMPLANT SYSTEMS | Whip-Mix Corp. | 2010-03-04 | 169 | 0 |
| K090976 | VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS | Whip-Mix Corp. | 2009-06-25 | 80 | 0 |
| K082299 | VERICORE IMPLANT ABUTMENTS | Whip-Mix Corp. | 2008-11-20 | 100 | 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