Data / Medical devices / Taiwan / Alliance Global Technology Co., Ltd.
Alliance Global Technology Co., Ltd.: FDA-registered device maker in Kaohsiung, Taiwan, 3 510(k) clearances
Alliance Global Technology Co., Ltd. is registered with the FDA (registration 3009325911) in Kaohsiung, Taiwan. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 2, 2016. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009325911
- Address
- 2F., No. 92 & 96, Luke 5th Rd., Kaohsiung Science Park, Luzhu Dist., Kaohsiung, Taiwan, 82151
- Owner or operator
- Alliance Global Technology Co., Ltd. (10045522)
- Roles
- Manufacturer
- First device listed
- November 26, 2013
- Registered through
- 2026
- Brand names listed
- ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS, ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS, DRILL, DENTAL, INTRAORAL, HANDLE, INSTRUMENT, DENTAL, IMPLANT, ENDOSSEOUS, ROOT-FORM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Manufacturer | accessdata.fda.gov |
| Handle, Instrument, Dental | EJB | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | 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 2, 2016 | K152576 | Anker II Dental Implant System | DZE | Substantially Equivalent | Alliance Global Technology Co., Ltd. | accessdata.fda.gov |
| September 21, 2015 | K142557 | Anker Dental Implant System - SB-III, ST and AT series | DZE | Substantially Equivalent | Alliance Global Technology Co., Ltd. | accessdata.fda.gov |
| November 14, 2013 | K131165 | ANKER DENTAL IMPLANT SYSTEM | DZE | Substantially Equivalent | Alliance Global | accessdata.fda.gov |
Compare with other makers
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Handle, Instrument, Dental
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Drill, Dental, Intraoral
Updated June 2, 2016. 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.