Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medo U.S.A., Inc. — Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K844064 | MEDO BUBBLE BATH MA-80, 400, 600 & 700 | Medo U.S.A., Inc. | 1985-01-23 | 97 | 0 |
| K841235 | MEDO MEDOMER MBF-100 II | Medo U.S.A., Inc. | 1984-11-19 | 242 | 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