Data / Medical devices / United States / Global Dental Technologies, Inc.
Global Dental Technologies, Inc.: FDA-registered device maker in Rogers, AR, United States, 2 510(k) clearances
Global Dental Technologies, Inc. is registered with the FDA (registration 3003929447) in Rogers, AR, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 7, 2006. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3003929447
- Address
- 101 N 37th St, Rogers, AR, United States, 72756
- Owner or operator
- GLOBAL DENTAL TECHNOLOGIES, INC. (9055957)
- Roles
- Repackager or relabeler
- First device listed
- April 17, 2003
- Registered through
- 2027
- Brand names listed
- ARTIFICIAL TEETH, Artificial Teeth, BIO HERADOR N, Denture, Plastic, Teeth, TILITE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alloy, Gold-Based Noble Metal | EJT | 2 | Repackager or relabeler | accessdata.fda.gov |
| Alloy, Metal, Base | EJH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Denture, Plastic, Teeth | ELM | 2 | Repackager or relabeler | accessdata.fda.gov |
| Teeth, Porcelain | ELL | 2 | Repackager or relabeler | 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 7, 2006 | K060507 | VALPLAST YAMAHACHI TEETH | ELM | Substantially Equivalent | Valplast Intl. Corp. | accessdata.fda.gov |
| December 28, 1982 | K823744 | PORCELAIN ARTIFICIAL TEETH | ELL | Substantially Equivalent | Dentsply Intl. | accessdata.fda.gov |
Compare with other makers
- All makers of Alloy, Metal, Base
- All makers of Teeth, Porcelain
- All makers of Denture, Plastic, Teeth
- All makers of Alloy, Gold-Based Noble Metal
Updated April 7, 2006. 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.