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CamX Triton HD, Cam Proxi

Model J2900 · DÜRR DENTAL SE · DI E247J29001

NTK — Light Transmission Caries Detector · Class II · 21 CFR 872.1745

UDILibrary device dossier · generated 2026-09-11 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

12232023-08: 0 reports for this device; peer average 2/device2023-10: 0 reports for this device; peer average 3/device2025-07: 0 reports for this device; peer average 1/device2025-09: 0 reports for this device; peer average 2/device08100709
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2023-0802
2023-1003
2025-0701
2025-0902
This device (reports/month)Average device in NTK (reports/device/month)

Regulatory clearances

  • K172007 SESE 2017-11-22 (k number procode)

Predicate lineage

K172007 — cites (transitively): K043068 (d1), K071429 (d1), K090169 (d1), K123402 (d1), K132953 (d1) — cited as predicate by K182712, K183471, K193644, K193659, K203703, K213482

Lineage extracted from public 510(k) summary text (heuristic).

Manufacturer compliance record — DÜRR DENTAL SE

Nothing in the loaded window.