Superdent® Pressure Indicator Paste

FDA UDI

Class I (US FDA UDI)

by Dentsply International

Identity

Trade Name: Superdent® Pressure Indicator Paste FDA UDI
Generic Name: Dental cement trial FDA UDI
Device Name: Superdent® Pressure Indicator Paste - 2 oz. - 951-8604 FDA UDI
Model / Reference: 1421101FG FDA UDI
Description: Superdent® Pressure Indicator Paste - 2 oz. - 951-8604 FDA UDI

Identifiers

Catalog Number: 1421101FG FDA UDI
Primary DI / UDI-DI: D6871421101FG2 FDA UDI
FDA Product Code: EFH FDA UDI
GMDN Term: Dental cement trial FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6140 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Total Volume — 59 Milliliter FDA UDI

Category: Dental cement trial

Superdent® Pressure Indicator Paste by Dentsply International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Mojo — KERR CORPORATION · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dentsply International

Sources (1)

FDA UDI bb06ca60-aa18-476a-b978-24c759b675e6 37 fields · synced Jun 8, 2026