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Evolve Matrix Procedure Kit

FDA UDI

by Bioclear Matrix Systems, LLC

Identity

Trade Name
Evolve Matrix Procedure Kit FDA UDI
Generic Name
Dental matrix band kit FDA UDI
Device Name
Convenience kit of Bioclear products used in posterior dental restorations. FDA UDI
Model / Reference
Brazil FDA UDI
Description
Convenience kit of Bioclear products used in posterior dental restorations. FDA UDI

Identifiers

Primary DI / UDI-DI
D9498270912 FDA UDI
GMDN Term
Dental matrix band kit FDA UDI

Classification

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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental matrix band kit

Evolve Matrix Procedure Kit by Bioclear Matrix Systems, LLC — 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 6d783bbc-6dd5-4baf-adc4-d8a31bb90a5a 33 fields · synced May 29, 2026