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Crane Dental Laboratory, Inc.

FDA Regulatory Profile

Crane Dental Laboratory, Inc. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 5, 2025 · NAI
Latest 510(k)
Sep 17, 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) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 5, 2025Rochester, NYDevicesNo Action Indicated (NAI)3010324114
Sep 1, 2022Rochester, NYDevicesNo Action Indicated (NAI)3010324114
Dec 18, 2018Rochester, NYDevicesNo Action Indicated (NAI)3010324114

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
K181416Sapphire Dorsal Comfort FitSep 17, 2019
K140429CRANE ACRYLIC HERBST APPLIANCESep 11, 2014

FDA data resources