Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Shenzhen Mareal Tech Co., Ltd. · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K220248 | Home use hair removal device | Shenzhen Mareal Tech Co., Ltd. | 2022-07-01 | 151 | 0 |
| K172883 | Home Use Hair Removal Device/T1, T2, T3 | Shenzhen Mareal Tech Co., Ltd. | 2018-02-12 | 144 | 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