Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
M.D. Intl., 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) |
|---|---|---|---|---|---|
| K894788 | DMI SERIES 90 EXAMINATION TABLE | M.D. Intl., Inc. | 1989-09-08 | 42 | 0 |
| K894789 | DMI 250 SERIES POWER SURGERY TABLE | M.D. Intl., Inc. | 1989-08-29 | 32 | 0 |
| K870832 | OXY-THERM | M.D. Intl., Inc. | 1987-03-12 | 9 | 0 |
| K771249 | JOY LIGHT | M.D. Intl., Inc. | 1977-07-15 | 8 | 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