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Dentorium

FDA UDI

Class I (US FDA UDI)

by Wright Health Group , Ltd.

Identity

Trade Name
Dentorium FDA UDI
Generic Name
Dental base plate FDA UDI
Device Name
Base Plates / Special Impression Tray Blanks. Shellac resin. Single thickness. Pink. Lower. FDA UDI
Model / Reference
Lower Single Pink x12 FDA UDI
Description
Base Plates / Special Impression Tray Blanks. Shellac resin. Single thickness. Pink. Lower. FDA UDI

Identifiers

Catalog Number
DS701 FDA UDI
Primary DI / UDI-DI
05056079042149 FDA UDI
FDA Product Code
EBH FDA UDI
GMDN Term
Dental base plate FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3670 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 base plate

Dentorium by Wright Health Group , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental base plate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afbd0d52-9c12-4cf3-832c-e2c36551f1d9 35 fields · synced May 30, 2026