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Dgh Technology, Inc.

FDA Regulatory Profile

Dgh Technology, Inc. has 0 FDA recalls, 4 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 22, 2024 · NAI
Latest 510(k)
Jul 31, 2017

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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) clearances7Oct 4, 2026Not statedCurrent
Inspections4Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 22, 2024Exton, PADevicesNo Action Indicated (NAI)2522950
Aug 3, 2016Exton, PADevicesVoluntary Action Indicated (VAI)2522950
Nov 22, 2013Exton, PADevicesNo Action Indicated (NAI)2522950
Dec 22, 2010Exton, PADevicesNo Action Indicated (NAI)2522950

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
K171301Scanmate FlexJul 31, 2017
K093371MODEL DGH 6000 SCANMATE AApr 5, 2010
K033385DGH 55 HANDHELD PACHYMETER (PACHMATE)Nov 7, 2003
K965127DGH MODEL 9000Mar 17, 1997
K920906DGH-500 PACHYMETERNov 2, 1992
K913067DGH-4000 A-SCAN/PACHYMETERJan 31, 1992
K872726DGH-3000A A-SCANDec 4, 1987

FDA data resources