Dental Device Guide
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Not currently registered with FDA under this name

Interpore Intl.

Irvine, CA, United States. Named as applicant on 22 dental 510(k) clearances between 1984 and 1997. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
221984–1997
Markets registered in
1United States
Establishments
0—
1984: 31986: 31987: 11988: 11990: 21991: 11992: 31994: 21995: 21996: 31997: 119801990200020102020

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Interpore Intl. as the applicant.

Decided510(k)DeviceDevice type
30 Oct 1997K972842INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGELYC Synthetic Bone Grafting Material
24 May 1996K960945IMZ MEMBRANE TACK SYSTEMDZL Intraosseous Fixation Screw
8 Mar 1996K960371INTERPORE THREADED IMPLANTDZE Root-Form Endosseous Implant
30 Jan 1996K955492INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLTDZE Root-Form Endosseous Implant
21 Nov 1995K952167IMZ BONE TACK SYSTEMDZL Intraosseous Fixation Screw
28 Mar 1995K950165INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID FILLERS, 425 TO 1000 MICRONS AND 425 TO 600 MICRONSLYC Synthetic Bone Grafting Material
25 Jul 1994K922872INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM.DZE Root-Form Endosseous Implant
10 Feb 1994K922732INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETERDZE Root-Form Endosseous Implant
13 Oct 1992K913228INTERPORE IMZ CYLINDER IMPLANT SYSTEMDZE Root-Form Endosseous Implant
22 Jun 1992K921246IMZ SURGICAL INSTRUMENT TRAYDZE Root-Form Endosseous Implant
8 Jan 1992K912734INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTSDZE Root-Form Endosseous Implant
5 Feb 1991K904611INTERPORE CYLINDRICAL HEX IMPLANTDZE Root-Form Endosseous Implant
27 Jul 1990K900793INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEMDZE Root-Form Endosseous Implant
26 Jul 1990K901928INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACHEGG All Precision Attachment
17 Nov 1988K883211IMZ O-RING ATTACHMENTDZE Root-Form Endosseous Implant
2 Mar 1987K870331IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTSEGG All Precision Attachment
24 Oct 1986K863680IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTSDZE Root-Form Endosseous Implant
23 May 1986K860983INTERPORE 200 POROUS HYDROXYAPATITELYC Synthetic Bone Grafting Material
3 Mar 1986K855032IMZ INTRAMOBILE CYLINDER IMPLANTDZE Root-Form Endosseous Implant
1 Oct 1984K843154TOOTH ROOT SOCKET GAUGELYC Synthetic Bone Grafting Material
27 Sep 1984K843153ANTERIOR ALVEOLAR RIDGE SIZERLYC Synthetic Bone Grafting Material
3 Aug 1984K841201POROUS HYDROXYAPATITE BG200LYC Synthetic Bone Grafting Material

Some of these clearances are listed with FDA today by another company: Highridge Medical, LLC (2).

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.