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 Asahi KaseiLabelled 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 Levitronix with 11 510(k) clearances. The most recent is a 510(k) clearance dated Jun 20, 2011: CENTRIMAG RETURN CANNULA KIT.
| Jun 20, 2011 | CENTRIMAG RETURN CANNULA KITK110980 · DWF | 510(k) clearances |
| Jun 20, 2011 | CENTRIMAG DRAINAGE CANNULA KITK110983 · DWF | 510(k) clearances |
| Aug 27, 2010 | LEVITRONIX 2ND GENERATION CENTRIMAG PRIMARY CONSOLE, LEVITRONIX MONITORK102129 · DWA | 510(k) clearances |
| Jan 13, 2010 | LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLESK093832 · DWA | 510(k) clearances |
| Oct 8, 2009 | LEVITRONIX PEDIMAG BLOOD PUMP, MODEL 201-90052K090051 · KFM | 510(k) clearances |
| Jan 15, 2009 | LEVITRONIX, THORATEC CENTRIMAG BACK-UP CONSOLESK090004 · DWA | 510(k) clearances |
| Nov 26, 2008 | LEVITRONIX CENTRIMAG PRIMARY CONSOLE; THORATEC CANTRIMAG PRIMARY CONSOLEK083340 · DWA | 510(k) clearances |
| Jun 19, 2008 | LEVITRONIX CENTRIMAG PRIMARY CONSOLE, THORATEC CENTRIMAG PRIMARY CONSOLEK081221 · DWA | 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
