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Millennium Dental Technologies, Inc.

FDA Regulatory Profile

Millennium Dental Technologies, Inc. has 0 FDA recalls, 1 inspection, 5 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 2, 2011 · NAI
Latest 510(k)
Jul 12, 2019

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances5Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 2, 2011Cerritos, CADevicesNo Action Indicated (NAI)3002690217

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K182930PerioLase Nd:YAG Pulsed Dental Laser SystemJul 12, 2019
K151763PerioLase Nd:YAG Pulsed Dental Laser SystemMar 15, 2016
K030290PERIOLASE ND:YAG DENTAL LASER SYSTEMJul 26, 2004
K014272PERIOLASE ND:YAG DENTAL LASER SYSTEMMar 27, 2002
K010771PERIOLASE ND:YAG DENTAL LASER SYSTEMNov 27, 2001

FDA data resources