Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of GetingeLabelled 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 14, 2026, FDA's public records list Jostra AG with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jan 30, 2004: JOSTRA SUCKERS, MODEL JS.
| Jan 30, 2004 | JOSTRA SUCKERS, MODEL JSK020983 · DWF | 510(k) clearances |
| Aug 7, 2003 | HEATER COOLER UNIT, MODEL HCU 30K031544 · DWC | 510(k) clearances |
| Feb 26, 2003 | QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030K030264 · DTZ | 510(k) clearances |
| Jan 9, 2003 | JOSTRA SINGLE STAGE VENOUS RETURN CATHETERSK020784 · DWF | 510(k) clearances |
| Dec 17, 2002 | JOSTRA MECC SYSTEMK023132 · KFM | 510(k) clearances |
| Sep 11, 2002 | JOSTRA VENT CATHETERS, MODELS LV & HKVK022022 · DWF | 510(k) clearances |
| Apr 24, 2002 | JOSTRA ANTEGRADE CARDIOPLEGIA CANNULAK020515 · DWF | 510(k) clearances |
| Mar 26, 2002 | JOSTRA RETROGRADE CARDIOPLEGIA CANNULAEK014303 · DWF | 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
