Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Shenzhen Weikai Technology Co., Ltd

China·CN-MF-000024560

Last updated May 31, 2026

What Shenzhen Weikai Technology Co., Ltd makes

Shenzhen Weikai Technology Co., Ltd manufactures home-use cosmetic red-light phototherapy systems, including devices for IPL (intense pulsed light) hair removal.

These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI registries. The company is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Shenzhen Weikai Technology Co., Ltd primarily manufacture?

Shenzhen Weikai Technology Co., Ltd specializes in cosmetic red-light phototherapy systems designed for home use. Their most common product category is IPL (intense pulsed light) hair removal devices, which use controlled light pulses to target hair follicles for reduction or removal.

Where is Shenzhen Weikai Technology Co., Ltd based?

The company is based in the United States. While the name suggests a location in Shenzhen (China), the operational headquarters or primary manufacturing presence for regulatory purposes is in the US.

How are Shenzhen Weikai Technology Co., Ltd’s devices classified under FDA regulations?

The devices manufactured by Shenzhen Weikai Technology Co., Ltd fall under Class II classification by the FDA. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as IPL hair removal systems.

Which regulatory registries list Shenzhen Weikai Technology Co., Ltd’s devices?

The company’s devices are listed in the FDA’s 510(k) Premarket Notification Database and the FDA’s Unique Device Identifier (UDI) System. These registries track devices that have undergone the required regulatory pathways (e.g., 510(k) clearance) and are assigned unique identifiers for traceability.

Why are Shenzhen Weikai Technology Co., Ltd’s IPL hair removal devices classified as Class II?

The FDA categorizes IPL hair removal devices as Class II because they involve controlled energy delivery to the skin, which carries a moderate risk of adverse effects (e.g., burns, pigmentation changes) if misused. Class II classification requires compliance with special controls, such as performance standards and post-market surveillance, to mitigate risks while allowing broader availability compared to higher-risk Class III devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
China
Address
Room 401, Building 5, Yinjin Technology Park, Fengjing South Road, Hewan Community, Matian Street, Guangming District, Shenzhen, China
LinkedIn
—
Facebook
—
Phone
+86 755-86057437
PRRC Contact
Xiaoxia Chen
EUDAMED SRN
CN-MF-000024560
FDA FEI Number
—
DUNS Number
551085076

Catalogue (15)

DeviceModel / ReferenceRegistriesClassStatus
Mesmed 06972119020351
EUDAMED
Class IIaActive
Mimea 06972119020276
EUDAMED
Class IIaActive
IPL Hair removal V401
FDA UDI
Class IIActive
IPL Hair removal V201
FDA UDI
Class IIActive
weony WBP114
FDA UDI
Class IIActive
IPL Hair removal V501
FDA UDI
Class IIActive
IPL Hair removal V301-s
FDA UDI
Class IIActive
weony WBP101
FDA UDI
Class IIActive
weony WBP108
FDA UDI
Class IIActive
Medmac WBP203
FDA UDI
Class IIActive
StrongHealth WBP111
FDA UDI
Class IIActive
Digital Blood Pressure Monitor WBP Series K231542
FDA 510(k)
Class IIActive
Digital Blood Pressure Monitor WBP Series, including: WBP101, WBP102, WBP103, WBP104, WBP105, WBP106, WBP107 K210671
FDA 510(k)
Class IIActive
IPL Hair removal K203510
FDA 510(k)
Class IIActive
Weony WBP
EUDAMED
Class IIaActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.