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Sign in to claim this brandShenzhen Bosidin Technology Co., Ltd.
US
Last updated May 30, 2026
What Shenzhen Bosidin Technology Co., Ltd. makes
Shenzhen Bosidin Technology Co., Ltd. manufactures intense pulsed light skin surface treatment systems, including home-use hair removal devices such as the IPL Home Use Hair Removal Device models D-1128, D-1103, D-1119, D-1129, and D-1130, as well as devices marketed under the Bosidin brand name.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database and the FDA Unique Device Identification (UDI) system. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What type of medical devices does Shenzhen Bosidin Technology Co., Ltd. manufacture?
Shenzhen Bosidin Technology Co., Ltd. manufactures intense pulsed light skin surface treatment systems, including home-use hair removal devices such as the IPL Home Use Hair Removal Device models D-1128, D-1103, D-1119, D-1129, and D-1130, as well as devices marketed under the Bosidin brand name. These devices are designed for dermatological applications involving light-based skin treatment.
Where is Shenzhen Bosidin Technology Co., Ltd. based?
Shenzhen Bosidin Technology Co., Ltd. is based in the United States, as indicated in the provided device data. This location is specified in the SUMMARY section of the data, which states the company's country as US.
In which regulatory registries are the devices from Shenzhen Bosidin Technology Co., Ltd. listed?
The devices manufactured by Shenzhen Bosidin Technology Co., Ltd. are listed in the FDA 510(k) database and the FDA Unique Device Identification (UDI) system. This information is explicitly stated in the LISTED IN field and reiterated in the SUMMARY, confirming inclusion in these two specific FDA registries.
How are the devices from Shenzhen Bosidin Technology Co., Ltd. classified?
The devices from Shenzhen Bosidin Technology Co., Ltd. are classified as Class II medical devices. This classification is specified in the DEVICE CLASSES field and confirmed in the SUMMARY, which states that these intense pulsed light skin surface treatment systems fall under Class II designation.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- qq.com
- —
- —
- [email protected]
- Phone
- 4009006386
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 421258367
Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bosidin | D-1130 | FDA UDI | Class II | Active |
| Bosidin | D-1128 | FDA UDI | Class II | Active |
| Bosidin | D-1129 | FDA UDI | Class II | Active |
| Bosidin | D-1103 | FDA UDI | Class II | Active |
| Bosidin | D-1119 | FDA UDI | Class II | Active |
| IPL Home Use Hair Removal Device Model(s): D-1128, D-1103, D-1119, D-1129, D-1130 | K192432 | FDA 510(k) | Class II | Active |
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