Interpore Intl.
Interpore Intl. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1998.
Top product codes for Interpore Intl.
Recent clearances by Interpore Intl.
- K981253 — ULTRACON ULTRAFILTRATOR
- K980817 — PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L
- K972842 — INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE
- K971036 — ODONTIT AUTOGENOUS BONE COLLECTION DEVICE
- K960945 — IMZ MEMBRANE TACK SYSTEM
- K960371 — INTERPORE THREADED IMPLANT
- K955492 — INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT
- K952167 — IMZ BONE TACK SYSTEM
- K950165 — INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID FILLERS, 425 TO 1000 MICRONS AND 425 TO 600 MICRONS
- K922872 — INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM.
- K922732 — INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER
- K913228 — INTERPORE IMZ CYLINDER IMPLANT SYSTEM
- K921246 — IMZ SURGICAL INSTRUMENT TRAY
- K912734 — INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTS
- K904611 — INTERPORE CYLINDRICAL HEX IMPLANT
- K900793 — INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM
- K901928 — INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH
- K883211 — IMZ O-RING ATTACHMENT
- K870331 — IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS
- K863680 — IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS
- K860983 — INTERPORE 200 POROUS HYDROXYAPATITE
- K855032 — IMZ INTRAMOBILE CYLINDER IMPLANT
- K843154 — TOOTH ROOT SOCKET GAUGE
- K843153 — ANTERIOR ALVEOLAR RIDGE SIZER
- K841201 — POROUS HYDROXYAPATITE BG200
Data sourced from openFDA. This site is unofficial and independent of the FDA.