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Xios XG Supreme

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name
Xios XG Supreme FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
XIOS AE REPLACEABLE CABLE KIT, 90CM FDA UDI
Model / Reference
6724772 FDA UDI
Description
XIOS AE REPLACEABLE CABLE KIT, 90CM FDA UDI

Identifiers

Catalog Number
6724772 FDA UDI
Primary DI / UDI-DI
D00367247721 FDA UDI
FDA Product Code
MQB FDA UDI
EAP FDA UDI
GMDN Term
Dental digital imaging sensor, intraoral FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 FDA UDI
872.1810 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental digital imaging sensor, intraoral

Xios XG Supreme by Dentsply International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental digital imaging sensor, intraoral.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 832dde47-9a95-4607-8b23-b7f56c4d97c2 34 fields · synced May 31, 2026