Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Beijing Honkon Technologies Co., Ltd. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
216 daysmedian FDA review time
308 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K161892 | Slimming Treatment Device | Beijing Honkon Technologies Co., Ltd. | 2017-03-02 | 234 | 0 |
| K131838 | DIODE LASER FOR HIAR REMOVAL | Beijing Honkon Technologies Co., Ltd. | 2014-04-24 | 308 | 0 |
| K131837 | CO2 FRACTIONAL LASER | Beijing Honkon Technologies Co., Ltd. | 2014-01-22 | 216 | 0 |
| K131857 | Q-SWITCHED ND:YAG LASER | Beijing Honkon Technologies Co., Ltd. | 2014-01-16 | 206 | 0 |
| K131859 | MULTIFUNCTIONAL SERIES | Beijing Honkon Technologies Co., Ltd. | 2013-10-18 | 116 | 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