Espe GmbH (Us) - FDA 510(k) Cleared Devices
59
Total
57
Cleared
0
Denied
FDA 510(k) Regulatory Record - Espe GmbH (Us) Dental ✕
58 devices
Cleared
Jun 18, 1993
PHOTAC-FIL APLICAP
Dental
259d
Cleared
Jan 14, 1992
SONO(R) -CEM
Dental
131d
Cleared
Jan 14, 1992
PHOTAC-BOND APLICAP, MODIFICATION
Dental
68d
Cleared
Dec 16, 1991
ROCATEC(R) -PLUS
Dental
111d
Cleared
Dec 04, 1991
ESPE(R) -SIL
Dental
90d
Cleared
Mar 29, 1991
VISIO-GEM ART-SYSTEM
Dental
108d
Cleared
Nov 19, 1990
PHOTAC-BOND
Dental
74d
Cleared
Nov 09, 1990
PHOTAC-BOND APLICAP
Dental
64d
Cleared
Nov 01, 1990
PERTAC UNIVERSAL BOND
Dental
45d
Cleared
Aug 09, 1990
PERTAC-HYBRID
Dental
188d
Cleared
Apr 10, 1990
PERTAC BOND
Dental
62d
Cleared
Mar 28, 1990
PROTEMP II
Dental
57d
Looking for a specific device from Espe GmbH (Us)? Search by device name or K-number.
Search all Espe GmbH (Us) devices