Data / Medical devices / China / Guangzhou Haoyimai Trading Co., Ltd.
Guangzhou Haoyimai Trading Co., Ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 1 510(k) clearance
Guangzhou Haoyimai Trading Co., Ltd. is registered with the FDA (registration 3014665853) in Guangzhou Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 6, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3014665853
- Address
- Room 508, Building 2, No. 383, Huangshi West Road, Baiyun District, Guangzhou, Guangdong, CHINA, Guangzhou Guangdong, China, 510440
- Owner or operator
- Guangzhou Haoyimai Trading Co., Ltd. (10095531)
- Roles
- Complaint file establishment, Exporter to the US, Foreign private label distributor
- First device listed
- March 25, 2026
- Registered through
- 2026
- Brand names listed
- COEROS WATER-BASED LUBRICANT (50ml,100ml,200ml,250ml,300ml), Pinknight Water-based lubricant, S Shock Shark 360ml,380ml,400ml,420ml,450ml,460ml,480ml,500ml,520ml,550ml,580ml,600ml,620ml,630ml,650ml,680ml,710ml,, S Shock Shark 50ml,60ml,80ml,100ml,120ml,140ml,150ml,160ml,180ml,200ml,240ml,250ml,260ml,280m,300ml,320ml,340ml,350ml,, S Shock Shark 720ml,740ml,750ml,760ml,780ml,800ml,850ml,900ml,946ml,1000ml
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Complaint file establishment, Exporter to the US, Foreign private label distributor | 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 |
|---|---|---|---|---|---|---|
| March 6, 2026 | K253983 | Water-based lubricant | NUC | Substantially Equivalent | Guangzhou Haoyimai Trading Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 6, 2026. 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.