Medical Device Manufacturer · DE , Pforzheim

Wieland Edelmetalle GmbH & Co. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2000

14

Total

14

Cleared

0

Denied

FDA 510(k) Regulatory Record - Wieland Edelmetalle GmbH & Co. Dental ✕

14 devices

1-14 of 14

Cleared Apr 24, 2002

AGC SPEZIALLEGIERUNG

Cleared Dec 31, 2001

AUROPAL, ORDER-NO.: 2101

Cleared Nov 20, 2001

DUO PAL 6, ORDER-NO.: 2154

Cleared Nov 02, 2001

PORTADUR P 2, MODEL #2031

Cleared Nov 01, 2001

BIOPORTA G, MODEL 2052

Cleared Nov 01, 2001

PORTA AURIUM, MODEL 2067

Cleared Nov 01, 2001

PORTA SMK 82, MODEL 2032

Cleared Nov 01, 2001

BIO PORTADUR, ORDER-NO.:2017

Cleared Nov 01, 2001

PORTA GEO TI MODEL #2004

Cleared Nov 01, 2001

PORTA MAXIMUM, MODEL# 2066

Cleared Oct 23, 2001

ERO50, ORDER-NO.: 2070

Cleared Oct 23, 2001

EURO 45, ORDER-NO.: 2064

Cleared Aug 16, 2001

Cleared May 23, 2000

AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED,...