Medical Device Manufacturer · US , Walker , MI

Interpore Intl. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1984

25

Total

25

Cleared

0

Denied

FDA 510(k) Regulatory Record - Interpore Intl. Dental ✕

22 devices

1-22 of 22

Cleared Oct 30, 1997

INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE

Cleared May 24, 1996

IMZ MEMBRANE TACK SYSTEM

Cleared Mar 08, 1996

INTERPORE THREADED IMPLANT

Cleared Jan 30, 1996

INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT

Cleared Nov 21, 1995

IMZ BONE TACK SYSTEM

Cleared Mar 28, 1995

INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID FILLERS, 425 TO...

Cleared Jul 25, 1994

INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM.

Cleared Feb 10, 1994

INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER

Cleared Oct 13, 1992

INTERPORE IMZ CYLINDER IMPLANT SYSTEM

Cleared Jun 22, 1992

IMZ SURGICAL INSTRUMENT TRAY

Cleared Jan 08, 1992

INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTS

Cleared Feb 05, 1991

INTERPORE CYLINDRICAL HEX IMPLANT

Cleared Jul 27, 1990

INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM

Cleared Jul 26, 1990

INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH

Cleared Nov 17, 1988

IMZ O-RING ATTACHMENT

Cleared Mar 02, 1987

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS

Cleared Oct 24, 1986

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS

Cleared May 23, 1986

INTERPORE 200 POROUS HYDROXYAPATITE

Cleared Mar 03, 1986

IMZ INTRAMOBILE CYLINDER IMPLANT

Cleared Oct 01, 1984

TOOTH ROOT SOCKET GAUGE

Cleared Sep 27, 1984

ANTERIOR ALVEOLAR RIDGE SIZER

Cleared Aug 03, 1984

POROUS HYDROXYAPATITE BG200