Beijing Honkon Technologies Co., Ltd.
Beijing, CN
BEIJING HONKON TECHNOLOGIES CO., LTD. appears in FDA device records in Beijing, CN. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Beijing Honkon Technologies Co., Ltd. between 2013 and 2017. The busiest year on record is 2014, with 3. The most recent is 2017, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2013 | 1 |
| 2014 | 3 |
| 2017 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K161892 | Slimming Treatment Device | NUV | Substantially Equivalent | |
| K131838 | DIODE LASER FOR HIAR REMOVAL | GEX | Substantially Equivalent | |
| K131837 | CO2 FRACTIONAL LASER | GEX | Substantially Equivalent | |
| K131857 | Q-SWITCHED ND:YAG LASER | GEX | Substantially Equivalent | |
| K131859 | MULTIFUNCTIONAL SERIES | ONF | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3009488834 | 3009488834 | BEIJING HONKON TECHNOLOGIES CO., LTD. | No.72 building, No.16 Huanke Middle Rd, Beijing 100176 CN | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain