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

1-12 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