Data / Medical devices / Thailand / Micro-Tech Medical Technology (Thailand) Co., Ltd.
Micro-Tech Medical Technology (Thailand) Co., Ltd.: FDA-registered device maker in Bang Lamung District Chon Buri, Thailand, 2 510(k) clearances
Micro-Tech Medical Technology (Thailand) Co., Ltd. is registered with the FDA (registration 3046205723) in Bang Lamung District Chon Buri, Thailand. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 30, 2015. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3046205723
- Address
- No. 966, 966/1, 966/2, 966/3, 966/4 Moo.3, Takian Tia Sub-district, Bang Lamung District Chon Buri, Thailand, 20150
- Owner or operator
- Micro-Tech (Nanjing) Co., Ltd. (9067602)
- Roles
- Manufacturer
- First device listed
- March 12, 2015
- Registered through
- 2027
- Brand names listed
- ADVANTIS Polypectomy Snare, Cold Snare, EdgeHog Polypectomy Snare, Injection Needle, LesionHunter Rotatable Nitinol Cold Snare, Pinpoint Injection Needle, Polypectomy Snare
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Endoscopic Injection Needle, Gastroenterology-Urology | FBK | 2 | Manufacturer | accessdata.fda.gov |
| Snare, Flexible | FDI | 2 | Manufacturer | accessdata.fda.gov |
| Snare, Surgical | GAE | 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 |
|---|---|---|---|---|---|---|
| July 30, 2015 | K150316 | Polypectomy Snare | FDI | Substantially Equivalent | Micro-Tech (Nanjing) Co., Ltd. | accessdata.fda.gov |
| June 2, 2015 | K150434 | Injection Needle | FBK | Substantially Equivalent | Micro-Tech (Nanjing) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Endoscopic Injection Needle, Gastroenterology-Urology
- All makers of Snare, Flexible
- All makers of Snare, Surgical
Updated July 30, 2015. 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.