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DEXIS Titanium Intraoral X-Ray Sensor

FDA UDI

Class II (US FDA UDI)

by Dental Imaging Technologies Corporation

Identity

Trade Name
DEXIS Titanium Intraoral X-Ray Sensor FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Model / Reference
1.012.6180 FDA UDI

Identifiers

Primary DI / UDI-DI
EKAV101261800 FDA UDI
510(k) Number
K172918 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
Dental digital imaging sensor, intraoral FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1800 FDA UDI
Commercial Distribution
Not 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

DEXIS Titanium Intraoral X-Ray Sensor by Dental Imaging Technologies Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K172918 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dental Imaging Technologies Corporation

Sources (1)

  • FDA UDI bd250b2f-4f7b-4460-8496-1a1ed5eb9a64 34 fields · synced Jun 9, 2026