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LumiGrip®

FDA UDI

Class I (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
LumiGrip® FDA UDI
Generic Name
Dental material application tool, single-use FDA UDI
Device Name
LUMIGrip KIT FDA UDI
Model / Reference
031752150 FDA UDI
Description
LUMIGrip KIT FDA UDI

Identifiers

Catalog Number
031752150 FDA UDI
Primary DI / UDI-DI
D8130317521500 FDA UDI
FDA Product Code
JEX FDA UDI
GMDN Term
Dental material application tool, 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

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

No

FDA UDI

Category: Dental material application tool, single-use

LumiGrip® by Den-Mat Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material application tool, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e075e16e-ae56-4f45-9cc5-5cc6da1b86ae 35 fields · synced Jun 9, 2026