Data / Medical devices / Thailand / Meiyume Manufacturing (Thailand) Limited
Meiyume Manufacturing (Thailand) Limited: FDA-registered device maker in LAMLUKKA Pathum Thani, Thailand, 1 510(k) clearance
Meiyume Manufacturing (Thailand) Limited is registered with the FDA (registration 3003823186) in LAMLUKKA Pathum Thani, Thailand. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 25, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003823186
- Address
- 21/7 Moo. 6 SUB-DIST.KOOKOT DISTRICT AREA, LAMLUKKA Pathum Thani, Thailand, 12130
- Owner or operator
- Meiyume Manufacturing (Thailand) Ltd (10050807)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- December 29, 2015
- Registered through
- 2026
- Brand names listed
- Durex 2 in 1 Massage Play Aloe Vera, Durex 2 in 1 Massage Play Guarana, Durex 2 in 1 Massage Play Ylang Ylang, Durex Cheeky Play Silicone Long Lasting Personal Lubricant, Durex Juicy Play Cherry Flavored Personal Lubricant, Durex Originals H2O, Durex Touch & Play Aloe Vera Massage & Pleasure Personal Lubricant, Durex Touch & Play Ylang Ylang Massage & Pleasure Personal Lubricant and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 2 | Contract manufacturer | accessdata.fda.gov |
| Lubricant, Personal | NUC | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| April 25, 2019 | K182100 | Smile Makers Personal Lubricant | NUC | Substantially Equivalent | Lfbeauty (Thailand) Limited | accessdata.fda.gov |
Compare with other makers
Updated April 25, 2019. 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.