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Cure-Thru Clear Cervical Matrices

FDA UDI

Class I (US FDA UDI)

by Premier Dental Products Company

Identity

Trade Name
Cure-Thru Clear Cervical Matrices FDA UDI
Generic Name
Dental matrix band, single-use FDA UDI
Device Name
CURE-THRU CMF BOX 150 - ANT/PRE FDA UDI
Model / Reference
9061017 FDA UDI
Description
CURE-THRU CMF BOX 150 - ANT/PRE FDA UDI

Identifiers

Primary DI / UDI-DI
00348783004830 FDA UDI
FDA Product Code
JEP FDA UDI
GMDN Term
Dental matrix band, single-use 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental matrix band, single-use

Cure-Thru Clear Cervical Matrices by Premier Dental Products Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental matrix band, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8f7c7afa-b0f9-4d2d-b291-b13edfaff394 33 fields · synced May 30, 2026