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DIAGNOdent 2095

FDA UDI

Class II (US FDA UDI)

by KaVo Dental GmbH

Identity

Trade Name
DIAGNOdent 2095 FDA UDI
Generic Name
Dental caries detector, optical induced fluorescence FDA UDI
Device Name
This is a medical device. FDA UDI
Model / Reference
0.574.0500 FDA UDI
Description
This is a medical device. FDA UDI

Identifiers

Catalog Number
2095 FDA UDI
Primary DI / UDI-DI
EKAV057405000 FDA UDI
FDA Product Code
NTK FDA UDI
GMDN Term
Dental caries detector, optical induced fluorescence FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1745 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

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

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 caries detector, optical induced fluorescence

DIAGNOdent 2095 by KaVo Dental GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental caries detector, optical induced fluorescence.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
KaVo Dental GmbH

Sources (1)

  • FDA UDI a3ebd105-8707-4fa7-990c-f0b666c44d80 36 fields · synced Jun 1, 2026