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Reel Matrix™

FDA UDI

Class I (US FDA UDI)

by Garrison Dental Solutions, L.l.c.

Identity

Trade Name
Reel Matrix™ FDA UDI
Generic Name
Dental matrix band, single-use FDA UDI
Device Name
Matrix Band, Dead-Soft FDA UDI
Model / Reference
RM200D FDA UDI
Description
Matrix Band, Dead-Soft FDA UDI

Identifiers

Catalog Number
RM200D FDA UDI
Primary DI / UDI-DI
10810038093175 FDA UDI
FDA Product Code
DZN 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 6.3 Millimeter FDA UDI

Category: Dental matrix band, single-use

Reel Matrix™ 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, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afbdd9ce-bfc2-4539-8dad-7ed597861aba 36 fields · synced Jun 8, 2026