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Duo-Gun

FDA UDI

Class I (US FDA UDI)

by DiaDent Group International

Identity

Trade Name
DUO-GUN FDA UDI
Generic Name
Endodontic obturation system FDA UDI
Device Name
Duo-Gun is an endodontic device that heat-soften specially-formulated Gutta Percha and enable vertical injection of softened Gutta Percha through the disposable obturation tip into the root canal. FDA UDI
Model / Reference
DUO-GUN BATTERY(1BL250DIA-3) FDA UDI
Description
Duo-Gun is an endodontic device that heat-soften specially-formulated Gutta Percha and enable vertical injection of softened Gutta Percha through the disposable obturation tip into the root canal. FDA UDI

Identifiers

Catalog Number
4007-2080 FDA UDI
Primary DI / UDI-DI
08806383586313 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Endodontic obturation system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endodontic obturation system

Duo-Gun by DiaDent Group International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic obturation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 568c3d20-022c-4f30-abe9-490ffd768b0c 35 fields · synced Jun 6, 2026