Registered with FDA
Arvit Dental Laboratory Inc.
Southampton, PA, United States. Lists 5 dental device types with FDA across 1 registered establishment.
- Device types listed
- 5
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Arvit Dental Laboratory Inc. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Resin Temporary Crown and BridgeEBG · Class 2 | Temporary crown & bridge materials | Lister | Crown and Bridge, Temporary, Resin | 2007 |
| Base Metal AlloyEJH · Class 2 | Dental alloys | Lister | BASE | 2006 |
| Gold-Based Noble Metal AlloyEJT · Class 2 | Dental alloys | Lister | GOLD-BASED NOBLE METAL | 2006 |
| Porcelain TeethELL · Class 2 | Dental ceramics & zirconia | Lister | Teeth, Porcelain | 2007 |
| Teeth Plastic DentureELM · Class 2 | Denture resins & teeth | Lister | Teeth, Denture, Plastic | 2007 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Arvit Dental Laboratory Inc. lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Dentsply Intl., Inc. (2), Dentsply International, Inc. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 17 Feb 2006 | K060293 | TEMPORARY CROWN AND BRIDGE MATERIAL | Dentsply International, Inc. | EBG Resin Temporary Crown and Bridge |
| 28 Dec 1982 | K823744 | PORCELAIN ARTIFICIAL TEETH | Dentsply Intl., Inc. | ELL Porcelain Teeth |
| 4 Jan 1980 | K792245 | TEETH, DENTURE, PLASTIC | Dentsply Intl., Inc. | ELM Teeth Plastic Denture |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| ARVIT DENTAL LABORATORY INC.FDA reg. 3006059056 | Southampton, PA, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9095679). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.