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G-Wedge™

FDA UDI

Class I (US FDA UDI)

by Garrison Dental Solutions, L.l.c.

Identity

Trade Name
G-Wedge™ FDA UDI
Generic Name
Dental matrix band kit FDA UDI
Device Name
Complete Wedge Assortment Kit: 400 Count (100 of Each Size) FDA UDI
Model / Reference
SPGWK4 FDA UDI
Description
Complete Wedge Assortment Kit: 400 Count (100 of Each Size) FDA UDI

Identifiers

Catalog Number
SPGWK4 FDA UDI
Primary DI / UDI-DI
00810038096124 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

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

Category: Dental matrix band kit

G-Wedge™ 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 3d2ff0b4-b424-4c2e-9b81-6d6b22fc52f0 35 fields · synced Jun 6, 2026