Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Lamidey Noury Medical · 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) |
|---|---|---|---|---|---|
| K240504 | PLASMA EDGE System | Lamidey Noury Medical | 2024-06-12 | 112 | 0 |
| K222542 | MCB UNIT Model: V10GMCBUS | Lamidey Noury Medical | 2022-09-21 | 30 | 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