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IPS InLine

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
IPS InLine FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
materials for inlays, onlays, crowns and bridges FDA UDI
Model / Reference
593212 FDA UDI
Description
materials for inlays, onlays, crowns and bridges FDA UDI

Identifiers

Catalog Number
593212 FDA UDI
Primary DI / UDI-DI
DIVO5932121 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental appliance fabrication material, ceramic

IPS InLine by Ivoclar Vivadent Aktiengesellschaft — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eedcf6e2-1707-47cd-a689-55b0bcfec8d1 34 fields · synced Jun 6, 2026