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Dual-Force™ Sectional Matrix System Ring Forceps

FDA UDI

Class I (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Dual-Force™ Sectional Matrix System Ring Forceps FDA UDI
Generic Name
Dental matrix band kit FDA UDI
Device Name
Sectional matrix ring placement instrument FDA UDI
Model / Reference
209009 FDA UDI
Description
Sectional matrix ring placement instrument FDA UDI

Identifiers

Catalog Number
209009 FDA UDI
Primary DI / UDI-DI
00359883004347 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental matrix band kit 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: Dental matrix band kit

Dual-Force™ Sectional Matrix System Ring Forceps by Den-Mat Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental matrix band kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b9570e41-2679-41fc-b37f-53eaa2d22a7b 35 fields · synced Jun 9, 2026