Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015422158

FEI Number

3015422158

Entity Name

ARTCRAFT DENTAL, INC.

City/State/Country

Dallas, TX, US

Establishment Address

6628 Warm Breeze Ln., Dallas, TX 75248, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

ArtCraft Dental, Inc. (Owner Number: 10060147)

Owner / Operator Contact Address

6628 Warm Breeze Ln., Dallas, TX 75248, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered 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

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EIS	Remover, Crown	Dental	Class 1	872.4565	2019-04-03
EMQ	Hoe, Periodontic	Dental	Class 1	872.4565	2020-12-04
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2019-04-03
JEX	Plier, Orthodontic	Dental	Class 1	872.4565	2024-12-16
EMK	Curette, Surgical, Dental	Dental	Class 1	872.4565	2019-04-03
PFL	Intraoral, Dental Foam Protector	Dental	Class 1	872.6890	2025-03-14
EJL	Bur, Dental	Dental	Class 1	872.3240	2024-12-16
EJI	Syringe, Cartridge	Dental	Class 2	872.6770	2024-12-16
EMD	Hemostat, Surgical	Dental	Class 1	872.4565	2019-04-03
EJB	Handle, Instrument, Dental	Dental	Class 1	872.4565	2019-04-03
EMG	Forceps, Tooth Extractor, Surgical	Dental	Class 1	872.4565	2019-04-03
EGN	Scissors, Surgical Tissue, Dental	Dental	Class 1	872.4565	2019-04-03

Official Correspondent

David Fyffe

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ArtCraft Dental, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K821275	Conphar, Inc.	MAYO SCISSOR STRAIGHT 5 1/2	1982-05-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015422158. Last updated year: 2026. Please use registration number 3015422158 when referencing this establishment in official correspondence.