Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Nusurg, Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
336 daysmedian FDA review time
582 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K924792 | MULTIPLE PURPOSE FORCEPS | Nusurg, Inc. | 1994-04-28 | 582 | 0 |
| K930610 | TALC DISPENSER SYRINGE | Nusurg, Inc. | 1993-11-04 | 272 | 0 |
| K924517 | AVITENE DISPENSER SYRINGE | Nusurg, Inc. | 1993-10-27 | 418 | 0 |
| K924372 | LAPAROSCOPIC NERVE HOOK | Nusurg, Inc. | 1993-07-30 | 336 | 0 |
| K924196 | LAPAROSCOPIC NEEDLE HOLDER | Nusurg, Inc. | 1993-06-25 | 309 | 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