FDA Registration Active 🇵🇭 Philippines

IVOCLAR VIVADENT, INC.

Reg #: 3004362235 · FEI: 3004362235 · Expires 2026
Products
4
Proprietary Names
53
Establishment Types
3
Classifications
4

Registration Details

Registration Name
IVOCLAR VIVADENT, INC.
Registration Number
3004362235
FEI Number
3004362235
Status
Active
Expiry Year
2026
Initial Importer
No
Address
#10 Ampere St., Light Industry & Science Park 1, Special Economic Processing Zone
City
Diezmo, Cabuyao City Laguna
Country
PH

Owner / Operator

Firm Name
IVOCLAR VIVADENT
Operator Number
8010208
Address
175 Pineview Dr.
City
Amherst
State
NY
Postal Code
14228
Country
US
Correspondent
Dana Glina

US Agent

Business Name
Ivoclar Vivadent
Contact Name
Anderjeet Gulati
Address
175 Pineview Dr.
City
Amherst
State
NY
ZIP
14228
Country
US
Phone
716 2642046

Products

Device Name Product Code
Powder, Porcelain EIH
Denture, Plastic, Teeth ELM
Instruments, Dental Hand DZN
Syringe, Restorative And Impression Material EID

Proprietary Names

IPS e.max ZirCAD Prime PREFERENCE PhysioStar NFC Plus Bonartic II NFC Plus Condyloform II NFC Plus Cavifil Injector OptraSculpt Instruments OptraStick SR ORTHOLINGUAL DCL SR VIVODENT DCL SR Orthotyp DCL Candulor brand denture teeth Candulor Physioset TCR Candulor Bonartic TCR BlueLine SR ORTHOPLANE DCL Virtual Dispenser Dispenser ZirCAD Cement Mixing Tips VivaPen Snap On Cannulas Vivadent Applicator Virtual Tips Variolink Application Tips Multilink Applicator Root Canal Tips Mixing Cannulas Intraoral Tips Mixing Tips SR Vivodent S PE SR Orthotyp S PE SR Vivodent S DCL SR Orthotyp S DCL SR Ortholingual S DCL PhysioSelect TCR BonSelect TCR Ivotion Dent SR Orthotyp Candulor brands SR Vivodent Preference Posterior SR Ivostar Preference Anterior SR Gnathostar SR Vivodent A-D SR Orthotyp A-D IPS InLine IPS Classic IPS InLine System Powder Opaquer IPS InLine One IPS Classic Powder Opaquer IPS e.max ZirCAD MT Multi blocks IPS e.max ZirCAD MT discs IPS e.max ZirCAD Prime Esthetic

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer) Export Device to the United States But Perform No Other Operation on Device Repack or Relabel Medical Device