Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Zmi Electronics , 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) |
|---|---|---|---|---|---|
| K241862 | Levina Pelvic Floor Muscle Stimulator (RS-48) | Zmi Electronics , Ltd. | 2025-03-27 | 273 | 0 |
| K231166 | Levina, Levina Incontinence Stimulation Electrodes (Sterile) | Zmi Electronics , Ltd. | 2024-01-18 | 268 | 0 |
| K180865 | ZMI Self-Adhesive Electrodes | Zmi Electronics , Ltd. | 2018-06-28 | 87 | 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