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 Integra LifeSciencesLabelled by claude-sonnet-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 MacroPore Biosurgery with 17 510(k) clearances. The most recent is a 510(k) clearance dated Sep 20, 2004: MACROPORE PURICEL LIPOPLASTY SYSTEM.
| Sep 20, 2004 | MACROPORE PURICEL LIPOPLASTY SYSTEMK042261 · QPB | 510(k) clearances |
| Jul 28, 2004 | MACROPORE HYDROSORB SPINE SYSTEMK041105 · KWQ | 510(k) clearances |
| Sep 22, 2003 | MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEETK031955 · FTL | 510(k) clearances |
| Sep 4, 2003 | MACROPORE CARDIO-WRAP (TS)K031785 · OMH | 510(k) clearances |
| Jul 1, 2003 | MACROPORE OS RECONSTRUCTIONK024169 · EZX | 510(k) clearances |
| Feb 21, 2003 | MACROPORE SURGICAL BARRIER FILMK023643 · MTZ | 510(k) clearances |
| Jul 1, 2002 | MACROPORE OS TRAUMAK021164 · HRS | 510(k) clearances |
| Dec 3, 2001 | MACROPORE SURGIWRAP (TS)K012025 · FTL | 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
