Guangdong Carain Beauty Equipment Co., Ltd.
Registered establishment in Foshan, Guangdong, China. 1 device type.
Guangdong Carain Beauty Equipment Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Powered Microneedle Device. Its earliest product listing with the FDA dates from 2020.
Registration
| Registered name | GUANGDONG CARAIN BEAUTY EQUIPMENT CO., LTD |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3011568699 |
| FEI number | 3011568699 |
| Establishment type | Contract manufacturer, Manufacturer |
Location
| City | Foshan |
|---|---|
| Province | Guangdong |
| Address | Room901-2, Bldg No.8 of CIMC High-tech Manufacturing Center, Chanxing 1st Rd, |
| Postal code | 528313 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Powered Microneedle Device | Class 2 | SkinStylus Microsystem, MRPen MicroSystem, SkinStylus SteriLock® Cartridge MicroSystem ( 4501), SkinStylus SteriLock® Cartridge 12pin ( 10445);, SkinStylus SteriLock® Cartridge Hilo ( SL38679);, SkinStylus SteriLock® Cartridge 36pin ( 10446); and 2 more | 2020 | 10 |
Clearances
No clearance names Guangdong Carain Beauty Equipment Co., Ltd. as applicant. 3 are held by other companies 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 |
|---|---|---|---|---|
| K241355 | 2024-10-09 | QAI | Traditional | SU-KO Technologies LLC |
| K222199 | 2022-10-21 | QAI | Traditional | Induction Therapies, LLC |
| K200044 | 2020-04-10 | QAI | Traditional | Esthetic Education, LLC |
From the Company
Published by the company on its own website, not by the FDA.
| Main products | Micro needle derma pen, RF thermage, Permanent makeup devices, Tattoo machines |
|---|---|
| Export markets | USA |
| OEM and ODM | Offered |
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.