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3D Dental

FDA UDI

Class I (US FDA UDI)

by 3d Dental Designs And Development, Llc

Identity

Trade Name
3D Dental FDA UDI
Generic Name
Dental matrix band, single-use FDA UDI
Device Name
Matrix Bands .002 12/Pk #13 FDA UDI
Model / Reference
MB02-13D FDA UDI
Description
Matrix Bands .002 12/Pk #13 FDA UDI

Identifiers

Catalog Number
MB02-13D FDA UDI
Primary DI / UDI-DI
00817169024699 FDA UDI
FDA Product Code
KCQ FDA UDI
GMDN Term
Dental matrix band, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6570 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

No

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 matrix band, single-use

3D Dental by 3d Dental Designs And Development, Llc — 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 e2daae29-7167-4953-ae5f-f491d96f0a48 34 fields · synced Jun 8, 2026