Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in AustraliaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Portland Orthopaedics Pty. Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 12, 2007: PORTLAND COBALT CHROME FEMORAL HEAD.
| Jan 12, 2007 | PORTLAND COBALT CHROME FEMORAL HEADK063278 · JDI | 510(k) clearances |
| Sep 1, 2006 | PORTLAND CERAMIC (BIOLOX-FORTE) FEMORAL HEADK061564 · LZO | 510(k) clearances |
| Jul 20, 2006 | M-COR HIP REPLACEMENT SYSTEMK053417 · LPH | 510(k) clearances |
| Oct 7, 2005 | EQUATOR PLUS ACETABULAR CUP SYSTEMK051844 · MAY | 510(k) clearances |
| Jan 20, 2004 | MODIFICATION TO: THE MARGRON HIP REPLACEMENT SYSTEMK032641 · MEH | 510(k) clearances |
| Feb 7, 2000 | THE MARGRON HIP REPLACEMENT SYSTEMK992815 · MEH | 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
