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Voco GmbH

Denver, CO, US

Voco GmbH appears in FDA device records in Denver, CO. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
12
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 12 510(k) clearances for Voco GmbH between 1991 and 1992. The busiest year on record is 1992, with 9. The most recent is 1992, with 9.

Clearances by year, as a table
510(k) clearance decisions for Voco GmbH, by decision year
YearClearances
19913
19929
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K924182CALCIMOL LCEJKSubstantially Equivalent
K924181POLIBONDKLESubstantially Equivalent
K923849CALCIMOLEJKSubstantially Equivalent
K922853AQUA IONOFILEMASubstantially Equivalent
K922854AQUA MERONEMASubstantially Equivalent
K920365TOOTH BONDING AGENTEBFSubstantially Equivalent
K915619IONOFIL/LONOFIL MOLAREMASubstantially Equivalent
K915618PROVICOLEMASubstantially Equivalent
K914612MERON DENTAL CEMENTEMASubstantially Equivalent
K914073F21(R) DENTAL CEMENTEMASubstantially Equivalent
K912497IONOBONDEMASubstantially Equivalent
K912495IONOSEALEJKSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

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