Manufacturer registered with FDA

Dental Crafters Inc.

Marshfield, WI, United States. Lists 3 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10030443Contract manufacturerManufacturer
Device types listed
3
Brands and models
8
510(k) clearances
12009–2009
Markets registered in
1United States
Establishments
1United States
2009: 1200020102020

510(k) clearances per year, 2000–2026

Devices listed with FDA

What Dental Crafters Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker
Biodenta Customized Abutments - TitaniumDESS Dental Smart SolutionsDESS Dental Smart Solutions - KeystoneGenesis ACTIVE AbutmentsK3Pro Customized Abutments
2017
Root-Form Endosseous ImplantDZE · Class 2Dental implantsMaker
Genesis ACTIVE AbutmentsK3Pro Customized Abutments
2017
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Surgical Guide
2020

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Dental Crafters Inc. as the applicant.

Decided510(k)DeviceDevice type
11 Sep 2009K090911IST SNORING APPLIANCELQZ Jaw Repositioning Device

Registered establishments

EstablishmentLocationWhat it does
DENTAL CRAFTERSFDA reg. 3004036186Marshfield, WI, United StatesContract manufacturer, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10030443). 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.