Data / Medical devices / United States / The Atlanta Dental Supply Company
The Atlanta Dental Supply Company: FDA-registered device maker in Duluth, GA, United States, 6 510(k) clearances
The Atlanta Dental Supply Company is registered with the FDA (registration 1013257) in Duluth, GA, United States. It lists 5 device types. The FDA files 6 510(k) clearances under its listings, the newest dated August 1, 2014. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 1013257
- Address
- 1650 Satellite Blvd, Duluth, GA, United States, 30097
- Owner or operator
- The Atlanta Dental supply Company (10060749)
- Roles
- Repackager or relabeler
- First device listed
- June 2, 2022
- Registered through
- 2026
- Brand names listed
- Admira Flow
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Agent, Tooth Bonding, Resin | KLE | 2 | Repackager or relabeler | accessdata.fda.gov |
| Cement, Dental | EMA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Material, Tooth Shade, Resin | EBF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Sealant, Pit And Fissure, And Conditioner | EBC | 2 | Repackager or relabeler | accessdata.fda.gov |
| Varnish, Cavity | LBH | 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 |
|---|---|---|---|---|---|---|
| August 1, 2014 | K141610 | FUTURABOND M+ | KLE | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
| December 21, 2011 | K113444 | N-HYBRIDE-COMPOSITE LC FLOW | EBF | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
| July 24, 2008 | K080814 | VOCO PROFLUORID VARNISH | LBH | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
| July 18, 2001 | K011756 | ADMIRA FLOW | EBF | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
| February 9, 1999 | K984097 | DC-CORE | EBF | Substantially Equivalent | S & C Polymer GmbH | accessdata.fda.gov |
| February 25, 1992 | K915618 | PROVICOL | EMA | Substantially Equivalent | Voco GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Agent, Tooth Bonding, Resin
- All makers of Sealant, Pit And Fissure, And Conditioner
- All makers of Material, Tooth Shade, Resin
- All makers of Cement, Dental
- All makers of Varnish, Cavity
Updated August 1, 2014. 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.