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Callisto Implant 78

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent, Inc.

Identity

Trade Name
Callisto Implant 78 FDA UDI
Generic Name
Dental casting noble alloy FDA UDI
Device Name
Callisto Implant 78 100g FDA UDI
Model / Reference
601951 FDA UDI
Description
Callisto Implant 78 100g FDA UDI

Identifiers

Catalog Number
601951 FDA UDI
Primary DI / UDI-DI
D7076019510 FDA UDI
FDA Product Code
EJT FDA UDI
GMDN Term
Dental casting noble alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3060 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Callisto Implant 78 by Ivoclar Vivadent, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 270863ea-990c-4f67-9c52-ed7ab84a9224 35 fields · synced Jun 9, 2026