Dongguan Bohuikang Technology Co., Ltd.
Manufacturer and brand owner in Dongguan, Guangdong, China. 4 device types, 1 product catalogued, 1 clearance.
Dongguan Bohuikang Technology Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Stimulator, Muscle, Powered, Stimulator, Nerve, Transcutaneous, For Pain Relief and 2 other device types. 1 of its products is catalogued under its own name. Its earliest product listing with the FDA dates from 2022.
Registration
| Registered name | DONGGUAN BOHUIKANG TECHNOLOGY CO.,LTD |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3023330992 |
| FEI number | 3023330992 |
| DUNS | 602493813 |
| Establishment type | Manufacturer |
Chinese Registration
| Chinese legal name | 东莞市博惠康科技有限公司 |
|---|---|
| Source | Qichacha company register |
Location
| City | Dongguan |
|---|---|
| Province | Guangdong |
| Address | 5th Floor,No 5, Second Street,Huaide Shui Xiang New Strict, Humen town |
| Postal code | 523165 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Stimulator, Muscle, Powered | Class 2 | Tens&EMS: KRES100D, KRES1010,KRES1020,KRES1080,KRES100B,AST1009,AST100B, KRES2080, 9029, KR-600, KR-800,KR-280, KR-300 | 2022 | 33 |
| Stimulator, Muscle, Powered, For Muscle Conditioning | Class 2 | Tens&EMS: KRES100D, KRES1010,KRES1020,KRES1080,KRES100B,AST1009,AST100B, KRES2080, 9029, KR-600, KR-800,KR-280, KR-300 | 2022 | 66 |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | Class 2 | Globalcare Micro 11 AND Microcare(Tens) | 2025 | 32 |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | Class 2 | Tens&EMS: KRES100D, KRES1010,KRES1020,KRES1080,KRES100B,AST1009,AST100B, KRES2080, 9029, KR-600, KR-800,KR-280, KR-300 | 2022 | 57 |
Own-Brand Listings
| Product | Code | Catalogue numbers |
|---|---|---|
| / | GZJ | 1 |
Clearances
1 clearance names Dongguan Bohuikang Technology Co., Ltd. as applicant. 1 is held by another company and named on this establishment’s own product listings: the device is cleared under that company’s 510(k) and listed under this registration.
| Clearance | Decision date | Product code | Route | Held by |
|---|---|---|---|---|
| K213788 | 2022-05-06 | NUH | Traditional | This company |
| K903394 | 1991-05-06 | GZJ | Traditional | Globalcare Medical Technology Co., Ltd. |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
The manufacturer named here can complete this record.