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Dentalis

FDA UDI

Class II (US FDA UDI)

by Neodental Chemical Products Co., Ltd.

Identity

Trade Name
Dentalis FDA UDI
Generic Name
Endodontic filling/sealing material FDA UDI
Device Name
Endodontic sealing material, 15g Powder, 10mL Liquid FDA UDI
Model / Reference
Set FDA UDI
Description
Endodontic sealing material, 15g Powder, 10mL Liquid FDA UDI

Identifiers

Primary DI / UDI-DI
04560128312585 FDA UDI
510(k) Number
K971642 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Endodontic filling/sealing material 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endodontic filling/sealing material

Dentalis by Neodental Chemical Products Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic filling/sealing material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dd5c20c1-26ab-40a1-b5af-7367f58bf81b 36 fields · synced Jun 8, 2026