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Specialites Septodont

Washington, DC, US

Specialites Septodont appears in FDA device records in Washington, DC. FDA records list 21 510(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
21
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 21 510(k) clearances for Specialites Septodont between 1985 and 2001. The busiest year on record is 1991, with 4. The most recent is 2001, with 2.

Clearances by year, as a table
510(k) clearance decisions for Specialites Septodont, by decision year
YearClearances
19852
19882
19893
19902
19914
19923
19983
20012
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K012427PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENTEATSubstantially Equivalent
K010415ISODANKLESubstantially Equivalent
K982773QUICKSET LIQUID AND POWDEREMASubstantially Equivalent
K982671SECURALLOYEJJSubstantially Equivalent
K980633ENDOSOLV EKIFSubstantially Equivalent
K920692SEPTOCALCINE ULTRAEJKSubstantially Equivalent
K915467CIMPAT S DENTAL CEMENTEMASubstantially Equivalent
K915466SEPTOPACK TEMPORARY FILLINGEBGSubstantially Equivalent
K913573SAFETY PLUS DENTAL INJECTION NEEDLEDZMSubstantially Equivalent
K913572AUTOPACK NON-EUGENOL PERIODONTAL DRESSINGEMASubstantially Equivalent
K913574SEPTOCAL CAVITY LINEREJKSubstantially Equivalent
K910735HEXIDIS ALCOHOL SWABLKBSubstantially Equivalent
K901082CYANODONT DENTAL CEMENTEMASubstantially Equivalent
K897095DISPOSINEEDLE SHARPS DISPOSAL UNITMMKSubstantially Equivalent
K895798SILCOT COPAL CAVITY VARNISHEMASubstantially Equivalent
K885007CIMPAT S TEMPORARY DENTAL CEMENTEMASubstantially Equivalent
K884653RACESTYPTINEEKJSubstantially Equivalent
K881890PROVISCEM OR PROVISCELL EUGENOL-FREE DENTAL CEMENTEMASubstantially Equivalent
K881661IONOSCEM OR IONOSCELL GLASS IONOMER DENTAL CEMENTEMASubstantially Equivalent
K851524SEPTOJECT STERILE DISPOSABLE INJECTION NEEDLEDZMSubstantially Equivalent
K851388SEPTOSIL SILICONE FOR PRECISION IMPRESSIONELWSubstantially 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