Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account
Interpore Intl. — Predicate Candidate Screening
25 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
449 days90th percentile
25clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K981253 | ULTRACON ULTRAFILTRATOR | Interpore Intl. | 1998-12-11 | 249 | 0 |
| K980817 | PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MOD | Interpore Intl. | 1998-09-25 | 206 | 0 |
| K972842 | INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE | Interpore Intl. | 1997-10-30 | 90 | 0 |
| K971036 | ODONTIT AUTOGENOUS BONE COLLECTION DEVICE | Interpore Intl. | 1997-06-03 | 75 | 0 |
| K960945 | IMZ MEMBRANE TACK SYSTEM | Interpore Intl. | 1996-05-24 | 77 | 0 |
| K960371 | INTERPORE THREADED IMPLANT | Interpore Intl. | 1996-03-08 | 42 | 0 |
| K955492 | INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT | Interpore Intl. | 1996-01-30 | 60 | 0 |
| K952167 | IMZ BONE TACK SYSTEM | Interpore Intl. | 1995-11-21 | 197 | 0 |
| K950165 | INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID | Interpore Intl. | 1995-03-28 | 70 | 0 |
| K922872 | INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 | Interpore Intl. | 1994-07-25 | 770 | 0 |
| K922732 | INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER | Interpore Intl. | 1994-02-10 | 612 | 0 |
| K913228 | INTERPORE IMZ CYLINDER IMPLANT SYSTEM | Interpore Intl. | 1992-10-13 | 449 | 0 |
| K921246 | IMZ SURGICAL INSTRUMENT TRAY | Interpore Intl. | 1992-06-22 | 98 | 0 |
| K912734 | INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTS | Interpore Intl. | 1992-01-08 | 202 | 0 |
| K904611 | INTERPORE CYLINDRICAL HEX IMPLANT | Interpore Intl. | 1991-02-05 | 117 | 0 |
| K900793 | INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM | Interpore Intl. | 1990-07-27 | 157 | 0 |
| K901928 | INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH | Interpore Intl. | 1990-07-26 | 90 | 0 |
| K883211 | IMZ O-RING ATTACHMENT | Interpore Intl. | 1988-11-17 | 111 | 0 |
| K870331 | IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS | Interpore Intl. | 1987-03-02 | 33 | 0 |
| K863680 | IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS | Interpore Intl. | 1986-10-24 | 35 | 0 |
| K860983 | INTERPORE 200 POROUS HYDROXYAPATITE | Interpore Intl. | 1986-05-23 | 67 | 0 |
| K855032 | IMZ INTRAMOBILE CYLINDER IMPLANT | Interpore Intl. | 1986-03-03 | 77 | 0 |
| K843154 | TOOTH ROOT SOCKET GAUGE | Interpore Intl. | 1984-10-01 | 52 | 0 |
| K843153 | ANTERIOR ALVEOLAR RIDGE SIZER | Interpore Intl. | 1984-09-27 | 48 | 0 |
| K841201 | POROUS HYDROXYAPATITE BG200 | Interpore Intl. | 1984-08-03 | 135 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda