Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sunmed, 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) |
|---|---|---|---|---|---|
| K062112 | SUNMED FOLEY CATHETERS | Sunmed, Inc. | 2007-06-04 | 315 | 0 |
| K955632 | ORTHOPLUG SOFT BONE DESIGN | Sunmed, Inc. | 1996-02-27 | 78 | 0 |
| K955631 | ORTHOPLUG HARD BONE DESIGN | Sunmed, Inc. | 1996-02-27 | 78 | 0 |
| K921263 | SUNLITE LARYNGOSCOPE | Sunmed, Inc. | 1993-06-01 | 442 | 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