HomeUSAWhip Mix Corporation

Whip Mix Corporation

USA · Louisville
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Saudi Arabia, Canada, Taiwan, Australia — 5 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
13listed device types
Class I 11Class II 1Class III 0unclassified 1
plus 12 registration records and 10 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
9registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
3active device licences
Class II 1Class III 2
4 including historic records
TWTaiwanTFDA
1valid device licences
Class I 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
6active ARTG entries
Class I 6
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States12 registration records, 10 510(k), 0 PMA
Saudi Arabia9 confirmed, 0 excluded
Canada3 confirmed, 0 excluded
Manufacturer names merged into this page: WHIP-MIX CORP. · WHIP MIX CORPORATION · Whip Mix Corporation

Company information

Country
USA
City
Louisville

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12008
12009
12010
42014
12016
12019
12025

FDA listed device types

showing 8 of 13
Plate, Base, Shellac 1Wax, Dental, Intraoral 1Positioner, Tooth, Preformed 1Tray, Impression, Preformed 1Facebow 1Accessories, Implant, Dental, Endosseous 1Forceps, Articulation Paper 1Material, Impression Tray, Resin 1

Registration details (sample)

MarketIdentifierNameClass / date
USK241729Hard Splint & Thermo-Adaptive Splint2025-03-18
USK190107VeriSplint2019-07-10
USK152443Vericore Gradient Temporary Disc2016-05-11
SAME0000011411SFDAA00012VERIGUIDE OS
SAME0000011411SFDAA00006Ulti-Mate Articulator
CA92844PREFERENCE SOFT DENTURE LINERClass II
CA96971VERICORE HTX ZIRCONIAClass III
CA99088WHIP MIX VERICORE (R) GRADIENT TEMPORARY DISCSClass III

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