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White Bite

FDA UDI

Class I (US FDA UDI)

by White Bite, Inc.

Identity

Trade Name
White Bite FDA UDI
Generic Name
Dental matrix band, reusable FDA UDI
Device Name
Pediatric Preformed Matrix Band 01 FDA UDI
Model / Reference
PB01 FDA UDI
Description
Pediatric Preformed Matrix Band 01 FDA UDI

Identifiers

Catalog Number
PB01 FDA UDI
Primary DI / UDI-DI
00850056330701 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

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 matrix band, reusable

White Bite by White Bite, 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

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Manufacturer

Manufacturer
White Bite, Inc.

Sources (1)

  • FDA UDI aa356a30-0d53-4a45-a009-40c823ff89aa 34 fields · synced Jun 8, 2026