Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Codan Medlon, 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) |
|---|---|---|---|---|---|
| K953958 | POWDERFREE BLUE LATEX EXAM GLOVES WITH PROTEIN CONTENT LABEL | Codan Medlon, Inc. | 1996-08-20 | 371 | 0 |
| K953956 | BLUE LATEX EXAM GLOVES WITH PROTEIN CONTENT LABELING CLAIM | Codan Medlon, Inc. | 1996-08-20 | 371 | 0 |
| K953955 | POWDERFREE LATEX EXAM GLOVES WITH PROTEIN CONTENT LABELING C | Codan Medlon, Inc. | 1996-08-20 | 371 | 0 |
| K960921 | CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE | Codan Medlon, Inc. | 1996-04-17 | 42 | 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