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Bioclear TwinRing Molar/Premolar Pack

FDA UDI

Class I (US FDA UDI)

by Bioclear Matrix Systems, LLC

Identity

Trade Name
Bioclear TwinRing Molar/Premolar Pack FDA UDI
Generic Name
Dental matrix band retainer FDA UDI
Device Name
Separator ring used in dental restorations. FDA UDI
Model / Reference
Molar/Premolar Pack FDA UDI
Description
Separator ring used in dental restorations. FDA UDI

Identifiers

Primary DI / UDI-DI
D9492080311 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental matrix band retainer 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental matrix band retainer

Bioclear TwinRing Molar/Premolar Pack by Bioclear Matrix Systems, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental matrix band retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6430b59f-c6ae-495a-b8b9-9abd041c177f 33 fields · synced May 30, 2026