Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Numed Technologies, Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
362 daysmedian FDA review time
645 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K922248 | MALLAWANY ATRAUMATIC TISSUE FORCEPS | Numed Technologies, Inc. | 1994-02-17 | 645 | 0 |
| K930571 | REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING | Numed Technologies, Inc. | 1994-02-01 | 362 | 0 |
| K931501 | NUMED DISPOSABLE ATT. NUMED HANDLE LAP. INST. | Numed Technologies, Inc. | 1994-01-11 | 292 | 0 |
| K923126 | MALLAWANY TISSUE GRASPING FORCEPS | Numed Technologies, Inc. | 1993-10-08 | 469 | 0 |
| K923055 | OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES | Numed Technologies, Inc. | 1992-11-23 | 152 | 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