Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Shenzhen Future Electronic Co., Ltd. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K251662 | Air Compression Therapy Device (ST-504); Air Compression The | Shenzhen Future Electronic Co., Ltd. | 2025-11-13 | 167 | 0 |
| K221092 | Transcutaneous Electrical Nerve Stimulator Model: ST-304 | Shenzhen Future Electronic Co., Ltd. | 2022-09-13 | 153 | 0 |
| K213745 | Air Compression Therapy Device, model: ST-502 | Shenzhen Future Electronic Co., Ltd. | 2022-03-31 | 122 | 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