Establishment registration
ARTCRAFT DENTAL, INC.
FDA establishment registration 3015422158 · Dallas, US
Key facts
| Registration number | 3015422158 |
|---|---|
| Establishment name | ARTCRAFT DENTAL, INC. |
| Owner/operator | ArtCraft Dental, Inc. |
| Owner/operator number | 10060147 |
| FEI number | 3015422158 |
| Address | 6628 Warm Breeze Ln. |
| City | Dallas |
| State | TX |
| Country | US |
| Establishment types | Specification developer, Single-use device reprocessor |
| Registration valid through | 2026 |
| Product codes listed | DZN, EGN, EIS, EIY, EJB, EJI, EJL, EMD, EMG, EMJ, EMK, EMQ, JEX, PFL |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database