Data / Medical devices / Thailand / Toppro International Co., Ltd.
Toppro International Co., Ltd.: FDA-registered device maker in Bangkok Krung Thep Maha Nakhon, Thailand, 1 510(k) clearance
Toppro International Co., Ltd. is registered with the FDA (registration 3042894943) in Bangkok Krung Thep Maha Nakhon, Thailand. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 18, 2019. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3042894943
- Address
- 1469/6 Soi Pattanakarn 31/1, Pattanakarn Road, Suanluang, Bangkok Krung Thep Maha Nakhon, Thailand, 10250
- Owner or operator
- Toppro International Co., Ltd. (10094969)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- January 11, 2026
- Registered through
- 2026
- Brand names listed
- MOTEX
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Surgeon'S Gloves | KGO | 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 |
|---|---|---|---|---|---|---|
| December 18, 2019 | K191898 | Sterile Latex Powder-Free Surgical Gloves | KGO | Substantially Equivalent | Modern Healthcare Corp. | accessdata.fda.gov |
Compare with other makers
Updated December 18, 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.