Wieland Edelmetalle GmbH & Co. is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Wieland Edelmetalle GmbH & Co. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Wieland Edelmetalle GmbH & Co. has 14 FDA 510(k) cleared dental devices. Based in Pforzheim, DE.
Historical record: 14 cleared submissions from 2000 to 2002.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wieland Edelmetalle GmbH & Co.
14 devices
Cleared
Apr 24, 2002
AGC SPEZIALLEGIERUNG
Dental
79d
Cleared
Dec 31, 2001
AUROPAL, ORDER-NO.: 2101
Dental
130d
Cleared
Nov 20, 2001
DUO PAL 6, ORDER-NO.: 2154
Dental
89d
Cleared
Nov 02, 2001
PORTADUR P 2, MODEL #2031
Dental
71d
Cleared
Nov 01, 2001
BIOPORTA G, MODEL 2052
Dental
70d
Cleared
Nov 01, 2001
PORTA AURIUM, MODEL 2067
Dental
70d
Cleared
Nov 01, 2001
PORTA SMK 82, MODEL 2032
Dental
70d
Cleared
Nov 01, 2001
BIO PORTADUR, ORDER-NO.:2017
Dental
70d
Cleared
Nov 01, 2001
PORTA GEO TI MODEL #2004
Dental
70d
Cleared
Nov 01, 2001
PORTA MAXIMUM, MODEL# 2066
Dental
70d
Cleared
Oct 23, 2001
ERO50, ORDER-NO.: 2070
Dental
61d
Cleared
Oct 23, 2001
EURO 45, ORDER-NO.: 2064
Dental
61d
Cleared
Aug 16, 2001
IMAGINE H.E.
Dental
36d
Cleared
May 23, 2000
AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED,...
Dental
53d