Wieland Edelmetalle GmbH & Co.
Wieland Edelmetalle GmbH & Co. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2002.
Top product codes for Wieland Edelmetalle GmbH & Co.
Recent clearances by Wieland Edelmetalle GmbH & Co.
- K020347 — AGC SPEZIALLEGIERUNG
- K012839 — AUROPAL, ORDER-NO.: 2101
- K012841 — DUO PAL 6, ORDER-NO.: 2154
- K012843 — PORTADUR P 2, MODEL #2031
- K012826 — BIOPORTA G, MODEL 2052
- K012827 — PORTA AURIUM, MODEL 2067
- K012828 — PORTA SMK 82, MODEL 2032
- K012831 — BIO PORTADUR, ORDER-NO.:2017
- K012834 — PORTA GEO TI MODEL #2004
- K012835 — PORTA MAXIMUM, MODEL# 2066
- K012838 — ERO50, ORDER-NO.: 2070
- K012840 — EURO 45, ORDER-NO.: 2064
- K012156 — IMAGINE H.E.
- K001041 — AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED, AGC-GOLDBONDER, AGC GLAVANOGOLD
Data sourced from openFDA. This site is unofficial and independent of the FDA.