Data / Medical devices / China / Shenzhen The World Of Chamerlain Trade Lmport And Export Co.,ltd.
Shenzhen The World Of Chamerlain Trade Lmport And Export Co.,ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen The World Of Chamerlain Trade Lmport And Export Co.,ltd. is registered with the FDA (registration 3043139371) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 9, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3043139371
- Address
- Room 201, Building 35, Lianchuang Science and Technology Park, No. 21 Bulan Road, Nanwan Subdistrict, Longgang, Shenzhen Guangdong, China, 518116
- Owner or operator
- Shenzhen The World of Chamerlain Trade lmport and Export Co. (10094801)
- Roles
- Manufacturer
- First device listed
- December 24, 2025
- Registered through
- 2026
- Brand names listed
- Drywell, Anal Discomfort Relief Serum, Model: L-31, Drywell, Anal Stimulation Enhancer Serum, Model: L-32, Drywell, Hyaluronic Acid Lubricant, Model: L-50, Drywell, Personal Lubricant, Model: L-10, L-11, Drywell, Refreshing Instant Surge Serum, Model: L-30
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | 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
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.