Espe GmbH & Co. Kg. is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Espe GmbH & Co. Kg. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Espe GmbH & Co. Kg. has 17 FDA 510(k) cleared dental devices. Based in Seefeld, DE.
Historical record: 17 cleared submissions from 1995 to 1998.
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 - Espe GmbH & Co. Kg.
17 devices
Cleared
Jan 29, 1998
POSITION PENTA, POSITION PENTA QUICK
Dental
78d
Cleared
Dec 22, 1997
SINFONY DENTIN, OPAQUE-DENTIN, ENAMEL, ENAMEL MODIFIER, TRANSPARENT...
Dental
96d
Cleared
Nov 17, 1997
KETAC-FIL APLICAP PLUS
Dental
80d
Cleared
Oct 02, 1997
CAVIT-LC
Dental
58d
Cleared
Nov 27, 1996
COJET SYSTEM
Dental
71d
Cleared
Nov 15, 1996
HYCEM APLICAP
Dental
59d
Cleared
Sep 12, 1996
EBS (ESPE BONDING SYSTEM)
Dental
80d
Cleared
Sep 11, 1996
PERTAC II/PERTAC II APLITIP
Dental
79d
Cleared
Sep 11, 1996
HYTAC APLITIP/HYTAC OSB
Dental
79d
Cleared
May 16, 1996
KETAC-MOLAR APLICAP
Dental
66d
Cleared
Mar 15, 1996
DIMENSION PENTA/DIMENSION GARANT L/POLYVINYL SILOXANE ADHESIVE
Dental
36d
Cleared
Dec 01, 1995
IMPREGUM PENTA
Dental
86d
Cleared
Nov 21, 1995
MICROGLISS
Dental
76d
Cleared
Aug 18, 1995
RAMITEC PENTA
Dental
66d
Cleared
Aug 18, 1995
PERMADYNE GARANT 2:1
Dental
31d
Cleared
Jul 19, 1995
PERMADYNE PENTA (HIGH & LOW VISCOSITY)
Dental
20d
Cleared
Feb 02, 1995
PROTEMP(R) GARANT
Dental
15d