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Wieland Edelmetalle GmbH & Co.

Pforzheim, DE

Wieland Edelmetalle GmbH & Co. appears in FDA device records in Pforzheim, DE. FDA records list 14 510(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
14
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 14 510(k) clearances for Wieland Edelmetalle GmbH & Co. between 2000 and 2002. The busiest year on record is 2001, with 12. The most recent is 2002, with 1.

Clearances by year, as a table
510(k) clearance decisions for Wieland Edelmetalle GmbH & Co., by decision year
YearClearances
20001
200112
20021
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K020347AGC SPEZIALLEGIERUNGEJTSubstantially Equivalent
K012839AUROPAL, ORDER-NO.: 2101EJTSubstantially Equivalent
K012841DUO PAL 6, ORDER-NO.: 2154EJSSubstantially Equivalent
K012843PORTADUR P 2, MODEL #2031EJTSubstantially Equivalent
K012835PORTA MAXIMUM, MODEL# 2066EJTSubstantially Equivalent
K012834PORTA GEO TI MODEL #2004EJTSubstantially Equivalent
K012831BIO PORTADUR, ORDER-NO.:2017EJTSubstantially Equivalent
K012828PORTA SMK 82, MODEL 2032EJSSubstantially Equivalent
K012827PORTA AURIUM, MODEL 2067EJTSubstantially Equivalent
K012826BIOPORTA G, MODEL 2052EJTSubstantially Equivalent
K012840EURO 45, ORDER-NO.: 2064EJSSubstantially Equivalent
K012838ERO50, ORDER-NO.: 2070EJTSubstantially Equivalent
K012156IMAGINE H.E.EIHSubstantially Equivalent
K001041AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED, AGC-GOLDBONDER, AGC GLAVANOGOLDEJTSubstantially 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