Manufacturer registered with FDA

Whip Mix Corporation

Louisville, KY, United States. Lists 12 dental device types with FDA across 1 registered establishment, and holds 8 510(k) clearances as applicant.

FDA owner/operator1043617ManufacturerRepacker / relabelerSpecification developer
Device types listed
12
Brands and models
18
510(k) clearances
82008–2016
Markets registered in
673 registrations outside the US
Establishments
1United States
2008: 12009: 12010: 12014: 42016: 1200020102020

510(k) clearances per year, 2000–2026

Registered in 6 markets

Where regulators' registries name Whip Mix Corporation as the manufacturer or the registration holder of a device.

All markets
United States: 12 device types listedCanada: 38 registrationsSouth Korea: 26 registrationsAustralia: 6 registrationsTaiwan: 2 registrationsUnited Kingdom: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerWhip Mix Corporation8 clearances2008–2016Below
CanadaHealth CanadaRegistration holderWHIP MIX CORPORATION382014–2019Pure Global AI
South KoreaMFDSManufacturerWhip Mix CorporationWhip-Mix Corporation · Whip-Mix corporation · +1261998–2014Pure Global AI
AustraliaTGAManufacturerWhip Mix Corporation62020–2025Pure Global AI
TaiwanTFDAManufacturerWHIP MIX CORPORATION22020–2021Pure Global AI
United KingdomMHRAManufacturerWhip Mix Corporation1—Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Whip Mix Corporation currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Resin Impression Tray MaterialEBH · Class 1Impression traysMaker
Denar Best Bite RegistrationVeriTRAY
2023
Rebasing Repairing Relining Denture ResinEBI · Class 2Denture resins & teethMaker
VeriSplint IOS
2019
Shellac Base PlateEEA · Class 1—Maker
VeriDENT Try-In
2023
Articulation PaperEFH · Class 1—Maker
ARDENT DENTAL ARTICULATING PAPERFILM
2007
Articulation Paper ForcepsEFK · Class 1Dental hand instrumentsLister
ARDENT DISPOSABLE DENT
2007
Intraoral Dental WaxEGD · Class 1—Lister
Denar Bite Reg wax
1992
Preformed Impression TrayEHY · Class 1Impression traysLister
VERITRAY
1977
ArticulatorsEJP · Class 1Articulators & facebowsMaker
DenarHanauWhip Mix Articulator
1992
Oral Cavity Abrasive Polishing AgentEJR · Class 1Polishing & prophylaxisMaker
PREPPIES FLOUR OF PUMICE
1997
FacebowKCR · Class 1Articulators & facebowsMaker
Cross RefFacebow for dentistryFacebow general
1992
Preformed Tooth PositionerKMY · Class 1Retainers, expanders & headgearMaker
VeriFIT Splint
2025
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Veriguide
2016

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 Whip Mix Corporation as the applicant.

Decided510(k)DeviceDevice type
11 May 2016K152443Vericore Gradient Temporary DiscEBG Resin Temporary Crown and Bridge
22 Oct 2014K142670Vericore Zirconia BlanksEIH Porcelain Powder
3 Sep 2014K140877VERICORE ZIRCONIA BLANKSEIH Porcelain Powder
29 Apr 2014K140146COMFORTSOFT SOFT DENTURE LINER SYSTEMEBI Rebasing Repairing Relining Denture Resin
26 Mar 2014K131760WHIP MIX PREPPIES PLUSEJR Oral Cavity Abrasive Polishing Agent
4 Mar 2010K092857VERICORE ABUTMENT IN TITANIUM FOR IMPLANT SYSTEMSNHA Endosseous Dental Implant Abutment
25 Jun 2009K090976VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMSNHA Endosseous Dental Implant Abutment
20 Nov 2008K082299VERICORE IMPLANT ABUTMENTSNHA Endosseous Dental Implant Abutment

Registered establishments

EstablishmentLocationWhat it does
WHIP-MIX CORP.FDA reg. 1043617LOUISVILLE, KY, United StatesManufacturer, Repacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 1043617). 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.