Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medmark, Inc. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K914498 | POWDER FREE, NON-STERILE, LATEX EXAMINATION GLOVES | Medmark, Inc. | 1991-11-27 | 50 | 0 |
| K894987 | MODEL #520/525 ED/RECOVERY STRETCHER | Medmark, Inc. | 1989-09-05 | 28 | 0 |
| K893949 | #157 EXAM LIGHT | Medmark, Inc. | 1989-08-07 | 67 | 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