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 LivaNovaLabelled 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 Sorin Biomedical Inc. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1999: MONOLYTH C 600 AND 1200 HOLLOW FIBER MEMBRANE LUNG WITH INTEGRATED SOFTSHELL VENOUS RESE….
| Nov 5, 1999 | MONOLYTH C 600 AND 1200 HOLLOW FIBER MEMBRANE LUNG WITH INTEGRATED SOFTSHELL VENOUS RESERVOIR , CVR 600 AND 1200 SOFTSHEK990103 · DTZ | 510(k) clearances |
| Feb 20, 1998 | DIDECO COMPACT-A AND COMPACT-M AUTOTRANSFUSION SYSTEMSK963759 · CAC | 510(k) clearances |
| Feb 20, 1998 | CODE 150 BLOOD COMPONENT COLLECTION SET AND WITH DIRECT DRAW LINEK963758 · CAC | 510(k) clearances |
| Sep 3, 1997 | VRF40 VENOUS RESERVOIR WITH INTEGRAL CARDIOTOMY FILTERK964908 · DTN | 510(k) clearances |
| Aug 21, 1997 | VENOMIDICARD PEDIATRIC VENOUS RESERVOIR WITH INTEGRALCARDIOTOMY FILTER/MIDICARD PEDIATRIC CARDIOTOMY RESERVOIR WITH FILTK964907 · DTN | 510(k) clearances |
| Aug 12, 1996 | DIDECO NEWBORN/INFANT ARTERIAL FILTERS: D735 MICRO 20 AND D736 MICRO 40K961869 · DTM | 510(k) clearances |
| Aug 21, 1995 | DIDECO ADULT ARTERIAL FILTERS D732 MICRO 20 W/20, D734 MICRO 40 W/40 MICRON SCREENK952270 · DTM | 510(k) clearances |
| Jun 27, 1995 | DIDECO PEDIATRIC ARTERIAL FILTERSK945198 · DTM | 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
