Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Zimmer BiometLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Interpore International with 25 510(k) clearances. The most recent is a 510(k) clearance dated Dec 11, 1998: ULTRACON ULTRAFILTRATOR.
| Dec 11, 1998 | ULTRACON ULTRAFILTRATORK981253 · FJI | 510(k) clearances |
| Sep 25, 1998 | PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30LK980817 · MQV | 510(k) clearances |
| Oct 30, 1997 | INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGEK972842 · LYC | 510(k) clearances |
| Jun 3, 1997 | ODONTIT AUTOGENOUS BONE COLLECTION DEVICEK971036 · GCY | 510(k) clearances |
| May 24, 1996 | IMZ MEMBRANE TACK SYSTEMK960945 · DZL | 510(k) clearances |
| Mar 8, 1996 | INTERPORE THREADED IMPLANTK960371 · DZE | 510(k) clearances |
| Jan 30, 1996 | INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLTK955492 · DZE | 510(k) clearances |
| Nov 21, 1995 | IMZ BONE TACK SYSTEMK952167 · DZL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
