Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Neomed Corp. · 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) |
|---|---|---|---|---|---|
| K790043 | TRACOR, CANNULA, BICEPTS BIPOLAR | Neomed Corp. | 1979-02-08 | 34 | 0 |
| K781810 | ELECTROSURGICAL UNIT 3001-3009 | Neomed Corp. | 1978-12-20 | 55 | 0 |
| K780118 | ELECTRODE, DISPERSIVE, DISP. NEOPAD | Neomed Corp. | 1978-02-23 | 31 | 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