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DEXIS Ti2 Sensor Kit

FDA UDI

Class II (US FDA UDI)

by Dental Imaging Technologies Corporation

Identity

Trade Name
DEXIS Ti2 Sensor Kit FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
DEXIS Ti2 Warranty Replacement NEW FDA UDI
Model / Reference
8.000.2578 FDA UDI
Description
DEXIS Ti2 Warranty Replacement NEW FDA UDI

Identifiers

Primary DI / UDI-DI
D090800025780 FDA UDI
510(k) Number
K233053 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
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

Yes

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

DEXIS Ti2 Sensor Kit by Dental Imaging Technologies Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental digital imaging sensor, intraoral.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 347b98bc-4731-4281-ac88-6c0957b04d46 34 fields · synced Jun 9, 2026