Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Fengh Medical Co., Ltd. · 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) |
|---|---|---|---|---|---|
| K242679 | Disposable Powered Articulating Endoscopic Linear Cutter Sta | Fengh Medical Co., Ltd. | 2024-10-04 | 28 | 0 |
| K202467 | Disposable Powered Articulating Endoscopic Linear Cutter Sta | Fengh Medical Co., Ltd. | 2020-12-14 | 109 | 0 |
| K182476 | Disposable Powered Articulating Endoscopic Linear Cutter Sta | Fengh Medical Co., Ltd. | 2019-12-18 | 464 | 0 |
| K180208 | Disposable Endoscopic Trocar | Fengh Medical Co., Ltd. | 2018-04-09 | 75 | 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