Data / Medical devices / China / Shenzhen Beston E-Commerce Co., Ltd
Shenzhen Beston E-Commerce Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Beston E-Commerce Co., Ltd is registered with the FDA (registration 3008469990) in Shenzhen Guangdong, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 9, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3008469990
- Address
- 3rd FI, building No.3 Guanghui Technology Park, minQing Road, Longhua District, Shenzhen Guangdong, China, 518110
- Owner or operator
- SHENZHEN BESTON E-COMMERCE CO., LTD (10059002)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- November 19, 2018
- Registered through
- 2027
- Brand names listed
- ADL100,AVB438,AVB439,AVB409,AVB400,AVB421,AVB425,AVB391,AVB427,AVB426,AVB403,AVB435,ADL099,AVB414, ALU011CL,ALU012CL,ALU013CL,ALU014CL,ALU015CL,ALU016CL,ALU017CL,ALU018CL, AMB084FL2L;AMB114WH;AMB109BL;A0061MF1001052L;AVB005BL-A, BST-A01;BST-A02;BST-A03;BST-A04;BST-A06;BST-A07;BST-A09;BST-A10;BST-A11, Bladder Control Devices/Kegel Exercise Weights(AKB001,AKB002,AKB003,AKB023PI), Massager BST-A05, BST-A05E, BST-A08, BST-A08E, BST-A13, BST-A13E, Massager BST-A12, BST-A12E, Masturbators(AMB112;AMB095;AMB113;AMB115) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cold Pack And Vibrating Massager | PHW | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Lubricant, Personal | NUC | 2 | Repackager or relabeler | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Vibrator For Therapeutic Use, Genital | KXQ | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 9, 2025 | K243107 | Water Solubility Human Body Lubricant | NUC | Substantially Equivalent | Dongguan Yanxuan Biotechnology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of Cold Pack And Vibrating Massager
- All makers of Vibrator, Therapeutic
- All makers of Massager, Therapeutic, Manual
- All makers of Vibrator For Therapeutic Use, Genital
- All makers of Lubricant, Personal
Updated May 9, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.