FDA Registration
Active
🇺🇸 United States
ARTCRAFT DENTAL, INC.
Reg #: 3015422158
·
FEI: 3015422158
·
Expires 2026
Products
14
Proprietary Names
19
Establishment Types
3
Classifications
14
Registration Details
- Registration Name
- ARTCRAFT DENTAL, INC.
- Registration Number
- 3015422158
- FEI Number
- 3015422158
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- Yes
- Address
- 6628 Warm Breeze Ln.
- City
- Dallas
- State
- TX
- ZIP
- 75248
- Country
- US
Owner / Operator
- Firm Name
- ArtCraft Dental, Inc.
- Operator Number
- 10060147
- Address
- 6628 Warm Breeze Ln.
- City
- Dallas
- State
- TX
- Postal Code
- 75248
- Country
- US
- Correspondent
- David D Fyffe
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Remover, Crown | EIS | Class 1 | Dental | No | 2019-04-03 |
| Hoe, Periodontic | EMQ | Class 1 | Dental | No | 2020-12-04 |
| Instruments, Dental Hand | DZN | Class 1 | Dental | No | 2019-04-03 |
| Plier, Orthodontic | JEX | Class 1 | Dental | No | 2024-12-16 |
| Curette, Surgical, Dental | EMK | Class 1 | Dental | No | 2019-04-03 |
| Intraoral, Dental Foam Protector | PFL | Class 1 | Dental | No | 2025-03-14 |
| Bur, Dental | EJL | Class 1 | Dental | No | 2024-12-16 |
| Syringe, Cartridge | EJI | Class 2 | Dental | No | 2024-12-16 |
| Hemostat, Surgical | EMD | Class 1 | Dental | No | 2019-04-03 |
| Handle, Instrument, Dental | EJB | Class 1 | Dental | No | 2019-04-03 |
| Forceps, Tooth Extractor, Surgical | EMG | Class 1 | Dental | No | 2019-04-03 |
| Scissors, Surgical Tissue, Dental | EGN | Class 1 | Dental | No | 2019-04-03 |
| Elevator, Surgical, Dental | EMJ | Class 1 | Dental | No | 2019-04-03 |
| Instrument, Filling, Plastic, Dental | EIY | Class 1 | Dental | No | 2020-12-04 |
Proprietary Names
TempOff
Molt Titanium
Max Crown Spreader
V-Plier
Serr8 Titanium
Crown Gripps
Metal Buster
702S
558S
PDL Gun
Castro-V
spotOn
Matrix Gripper
TraXion Forceps
Edge Ultra Scissor
Xpander
L-vator
Gold-N-Retriever
CompPlus
Establishment Types
Repack or Relabel Medical Device
Reprocess Single-Use Device
Develop Specifications But Do Not Manufacture At This Facility