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Composi-Tight®

FDA UDI

Class I (US FDA UDI)

by Garrison Dental Solutions, L.l.c.

Identity

Trade Name
Composi-Tight® FDA UDI
Generic Name
Dental matrix band kit FDA UDI
Device Name
3D Fusion™ Sectional Matrix System: (80) Original Matrices, (50) Wedges, (10) FenderWedge®, (1) FX500 Tall Ring, (1) Ring Placement Forceps FDA UDI
Model / Reference
UN32 FDA UDI
Description
3D Fusion™ Sectional Matrix System: (80) Original Matrices, (50) Wedges, (10) FenderWedge®, (1) FX500 Tall Ring, (1) Ring Placement Forceps FDA UDI

Identifiers

Catalog Number
UN32 FDA UDI
Primary DI / UDI-DI
00810038096353 FDA UDI
FDA Product Code
JEP 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental matrix band kit

Composi-Tight® by Garrison Dental Solutions, L.l.c. — 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 353568e8-92bc-41a4-a4f9-bcbd2730cda0 35 fields · synced Jun 8, 2026