Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Diversified Medical Instruments, 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) |
|---|---|---|---|---|---|
| K931814 | DMI UTERINE MOBILIZER/ELEVATOR/CANNULA | Diversified Medical Instruments, Inc. | 1994-05-31 | 418 | 0 |
| K926080 | DMI LAPAROSCOPIC IRRIGATION PUMP | Diversified Medical Instruments, Inc. | 1994-02-25 | 451 | 0 |
| K926078 | DMI TOCAR AND CANNULA SYSTEM | Diversified Medical Instruments, Inc. | 1993-05-17 | 167 | 0 |
| K926079 | DMI LAPAROSCOPIC ELECTRODES | Diversified Medical Instruments, Inc. | 1993-04-07 | 127 | 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