Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Shenzhen Jian Feng Electronic Technology 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) |
|---|---|---|---|---|---|
| K223825 | Tens & Ems Device | Shenzhen Jian Feng Electronic Technology Co., Ltd. | 2023-05-09 | 139 | 0 |
| K213741 | TENS & EMS DEVICE (Model: FM-B2403A) | Shenzhen Jian Feng Electronic Technology Co., Ltd. | 2022-03-08 | 99 | 0 |
| K213835 | TENS & EMS Device | Shenzhen Jian Feng Electronic Technology Co., Ltd. | 2022-03-03 | 84 | 0 |
| K202866 | TENS & EMS Device | Shenzhen Jian Feng Electronic Technology Co., Ltd. | 2021-05-19 | 233 | 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