Data / Medical devices / Thailand / STGT-TG 1
STGT-TG 1: FDA-registered device maker in Kantang Trang, Thailand, 2 510(k) clearances
STGT-TG 1 is registered with the FDA (registration 3020160813) in Kantang Trang, Thailand. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 24, 2011. Registered through 2027. 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
- 3020160813
- Address
- 85 Moo 6,Khuan Thani, Kantang Trang, Thailand, 92110
- Owner or operator
- SRI TRANG GLOVES (THAILAND) PUBLIC COMPANY LIMITED. (8041108)
- Roles
- Manufacturer
- First device listed
- November 29, 2017
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Latex Patient Examination Glove | LYY | 1 | 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 |
|---|---|---|---|---|---|---|
| June 24, 2011 | K111133 | NON-STERILE, POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CLAIM (50 MG OR LESS) | LYY | Substantially Equivalent | Ssc Surat Thani | accessdata.fda.gov |
| July 9, 2010 | K100907 | NON-STERILE, POWDER FREE LATEX EXAMINATION GLOVES AND PROTEIN CLAIM (50 MICROGRAMS OR LESS) MODEL: WHITE: X-SMALL, SMALL | LYY | Substantially Equivalent | Siam Sempermed Corp., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 24, 2011. 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.