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Pentron Clinical Technologies

Wallingford, CT, US

Pentron Clinical Technologies appears in FDA device records in Wallingford, CT. FDA records list 13 510(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
13
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 13 510(k) clearances for Pentron Clinical Technologies between 2002 and 2009. The busiest year on record is 2007, with 4. The most recent is 2009, with 1.

Clearances by year, as a table
510(k) clearance decisions for Pentron Clinical Technologies, by decision year
YearClearances
20021
20032
20052
20062
20074
20081
20091
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K091512BUILD-IT LIGHT CUREEBFSubstantially Equivalent
K081887LUTE-IT II VENEER CEMENT, MODEL NO6EMASubstantially Equivalent
K072830RM BOND, MODEL J032DYHSubstantially Equivalent
K072480GENERATION 8 SE ADHESIVEKLESubstantially Equivalent
K072545ARTISTE SE FLOWABLE COMPOSITE, MODEL N280EBFSubstantially Equivalent
K071500NANO-BOND II ADHESIVE SYSTEMKLESubstantially Equivalent
K060889SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SEKIFSubstantially Equivalent
K060698CEMENT-IT ALL PURPOSE, MODEL N97EMASubstantially Equivalent
K052106SIMILE FLOWEBFSubstantially Equivalent
K052349AVANTE LED CURING UNIT, MODEL N44EBZSubstantially Equivalent
K023818FIBERFILL AGPKIFSubstantially Equivalent
K023819FIBERFILL SGPEKMSubstantially Equivalent
K022150TRIONOMEREMASubstantially 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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What MDM checks, and what it does not

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