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DGH Technology, Inc.

Exton, PA, US

DGH TECHNOLOGY, INC. appears in FDA device records in Exton, PA. FDA records list 7 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
7
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 7 510(k) clearances for DGH Technology, Inc. between 1987 and 2017. The busiest year on record is 1992, with 2. The most recent is 2017, with 1.

Clearances by year, as a table
510(k) clearance decisions for DGH Technology, Inc., by decision year
YearClearances
19871
19922
19971
20031
20101
20171
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K171301Scanmate FlexIYOSubstantially Equivalent
K093371MODEL DGH 6000 SCANMATE AIYOSubstantially Equivalent
K033385DGH 55 HANDHELD PACHYMETER (PACHMATE)IYOSubstantially Equivalent
K965127DGH MODEL 9000HQCSubstantially Equivalent
K920906DGH-500 PACHYMETERIYOSubstantially Equivalent
K913067DGH-4000 A-SCAN/PACHYMETERIYOSubstantially Equivalent
K872726DGH-3000A A-SCANIYOSubstantially Equivalent

Registered establishments

FDA registered establishments for DGH Technology, Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
25229502522950DGH TECHNOLOGY, INC.110 SUMMIT DR., SUITE B, EXTON, PA 19341 US2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain