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CamX Triton HD, Cam Proxi

FDA UDI

Class II (US FDA UDI)

by Durr Dental AG

Identity

Trade Name
CamX Triton HD, Cam Proxi FDA UDI
Generic Name
Dental caries detector, optical induced fluorescence FDA UDI
Model / Reference
J2900 FDA UDI

Identifiers

Primary DI / UDI-DI
E247J29001 FDA UDI
510(k) Number
K172007 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

CamX Triton HD, Cam Proxi by Durr Dental AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental caries detector, optical induced fluorescence.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Durr Dental AG

Sources (1)

  • FDA UDI 98782b37-a9ac-4104-b1f3-c906e5b93c90 33 fields · synced Jun 8, 2026