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Model MO1-CT1 · Medit Corp. · DI 08800026700326

NOF — System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations · Class II · 21 CFR 872.3661

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.

12232021-02: 0 reports for this device; peer average 1.14/device2021-04: 0 reports for this device; peer average 1.14/device2023-09: 0 reports for this device; peer average 3/device2024-05: 0 reports for this device; peer average 3/device2024-06: 0 reports for this device; peer average 3/device2025-06: 0 reports for this device; peer average 1/device2025-12: 0 reports for this device; peer average 2/device02040905060612
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2021-0201.14
2021-0401.14
2023-0903
2024-0503
2024-0603
2025-0601
2025-1202
This device (reports/month)Average device in NOF (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — Medit Corp.

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