← Back to catalogue

Denovo Preformed Matrix Band

FDA UDI

Class I (US FDA UDI)

by Denovo Dental Inc

Identity

Trade Name
Denovo Preformed Matrix Band FDA UDI
Generic Name
Dental matrix band, reusable FDA UDI
Device Name
Denovo Preformed Matrix Band - Adult 1/4, Size 3 FDA UDI
Model / Reference
170-403 FDA UDI
Description
Denovo Preformed Matrix Band - Adult 1/4, Size 3 FDA UDI

Identifiers

Primary DI / UDI-DI
00810059290990 FDA UDI
FDA Product Code
JEP FDA UDI
GMDN Term
Dental matrix band, reusable 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental matrix band, reusable

Denovo Preformed Matrix Band by Denovo Dental Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental matrix band, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Denovo Dental Inc

Sources (1)

  • FDA UDI 956e732e-7b1b-44ce-b580-f91c840579a2 33 fields · synced May 30, 2026