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NeoPRO™

FDA UDI

Class II (US FDA UDI)

by US Endodontics, LLC

Identity

Trade Name
NeoPRO™ FDA UDI
Generic Name
Hygroscopic dental cement FDA UDI
Device Name
NeoPRO™ Bioceramic Sealer 0 FDA UDI
Model / Reference
NEOPRO2G FDA UDI
Description
NeoPRO™ Bioceramic Sealer 0 FDA UDI

Identifiers

Catalog Number
NEOPRO2G FDA UDI
Primary DI / UDI-DI
00818365026449 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Hygroscopic dental cement FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hygroscopic dental cement

NeoPRO™ by US Endodontics, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hygroscopic dental cement.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
US Endodontics, LLC

Sources (1)

  • FDA UDI 9e7840b6-5b37-41f0-9401-86aa4b9999af 35 fields · synced May 30, 2026