Data / Medical devices / United States / Arvit Dental Laboratory Inc.
Arvit Dental Laboratory Inc.: FDA-registered device maker in Southampton, PA, United States, 3 510(k) clearances
Arvit Dental Laboratory Inc. is registered with the FDA (registration 3006059056) in Southampton, PA, United States. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 17, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006059056
- Address
- 528 Street Rd. FL.1, Southampton, PA, United States, 18966
- Owner or operator
- ARVIT DENTAL LABORATORY INC. (9095679)
- Roles
- Repackager or relabeler
- First device listed
- December 15, 2006
- Registered through
- 2026
- Brand names listed
- BASE, Crown and Bridge, Temporary, Resin, GOLD-BASED NOBLE METAL, Teeth, Denture, Plastic, Teeth, Porcelain
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 |
| Crown And Bridge, Temporary, Resin | EBG | 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 |
|---|---|---|---|---|---|---|
| February 17, 2006 | K060293 | TEMPORARY CROWN AND BRIDGE MATERIAL | EBG | Substantially Equivalent | Dentsply International, Inc. | accessdata.fda.gov |
| December 28, 1982 | K823744 | PORCELAIN ARTIFICIAL TEETH | ELL | Substantially Equivalent | Dentsply Intl. | accessdata.fda.gov |
| January 4, 1980 | K792245 | TEETH, DENTURE, PLASTIC | ELM | Substantially Equivalent | Dentsply Intl. | accessdata.fda.gov |
Compare with other makers
- All makers of Denture, Plastic, Teeth
- All makers of Crown And Bridge, Temporary, Resin
- All makers of Teeth, Porcelain
- All makers of Alloy, Metal, Base
- All makers of Alloy, Gold-Based Noble Metal
Updated February 17, 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.