Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Everlife Medical Equipment 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) |
|---|---|---|---|---|---|
| K071624 | EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR | Everlife Medical Equipment Co., Ltd. | 2007-11-27 | 166 | 0 |
| K071320 | EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504 | Everlife Medical Equipment Co., Ltd. | 2007-08-17 | 99 | 0 |
| K070890 | EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507 | Everlife Medical Equipment Co., Ltd. | 2007-06-29 | 91 | 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