Medical Device Manufacturer · US , Mchenry , IL

Espe GmbH (Us) - FDA 510(k) Cleared Devices

59 submissions · 57 cleared · Since 1977

59

Total

57

Cleared

0

Denied

58 devices

26-50 of 58

Cleared Apr 12, 1988

KETAC-BOND APLICAP

Cleared Mar 09, 1988

KETAC-CONDITIONER

Cleared Mar 09, 1988

PERMADYNE ADHESIVE

Cleared Mar 09, 1988

IMPREGUM F ADHESIVE

Cleared Mar 01, 1988

Cleared Feb 26, 1988

Cleared Sep 15, 1987

MODIFIED VISIO-SEAL

Cleared Feb 19, 1987

ESPE CHELON-SILVER

Cleared Aug 18, 1986

ESPE VISIO-MOLAR

Cleared Mar 17, 1986

Cleared Feb 13, 1986

ESPE NIMETIC-GRIP

Cleared Aug 19, 1985

ESPE KETAC-BOND

Cleared Mar 25, 1985

ESPE KETAC-CEM RADIOPAQUE

Cleared Dec 06, 1984

Cleared Feb 03, 1984

Cleared Sep 28, 1982

Cleared Sep 14, 1982

Cleared Oct 22, 1979

Cleared Apr 30, 1979

KETAC APPLIC-CAPSULES

Cleared Apr 30, 1979

Cleared Nov 02, 1977

NIMETIC POLISHING PASTE

Cleared Oct 13, 1977

PERMAGUM ADHESIVE

Cleared Sep 06, 1977

Cleared Sep 02, 1977

Cleared Aug 03, 1977