Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medimix Products, Inc. · 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) |
|---|---|---|---|---|---|
| K914733 | TTL MEDICATED DRESSING | Medimix Products, Inc. | 1992-07-01 | 254 | 0 |
| K910664 | MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN. | Medimix Products, Inc. | 1992-04-01 | 412 | 0 |
| K902772 | PLEASURE PLUS | Medimix Products, Inc. | 1991-08-14 | 418 | 0 |
| K860113 | DOUBLE-JECT TRANSFER NEEDLE | Medimix Products, Inc. | 1986-02-12 | 30 | 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