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-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 Integra Neurocare, LLC with 12 510(k) clearances. The most recent is a 510(k) clearance dated Nov 2, 2000: VENTRIX TRUE TECH VENTRICULAR TUNNELING PRESSURE MONITORING KIT, MODEL NL960-V.
| Nov 2, 2000 | VENTRIX TRUE TECH VENTRICULAR TUNNELING PRESSURE MONITORING KIT, MODEL NL960-VK002392 · GWM | 510(k) clearances |
| Aug 17, 1999 | NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33K992006 · OCV | 510(k) clearances |
| May 26, 1999 | BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730)K981246 · JXG | 510(k) clearances |
| Dec 16, 1997 | MAURICE WORLDWIDE SHUNT SYSTEMK973525 · JXG | 510(k) clearances |
| Nov 3, 1997 | EXTERNAL CSF DRAINAGE MANAGEMENT SYSTEMSK972994 · JXG | 510(k) clearances |
| Sep 15, 1997 | RIVETTI-LEVINSON INSTRALUMINAL SHUNTK972261 · DWF | 510(k) clearances |
| Jul 31, 1997 | ENDOSCOPIC VENTRICULAR CATHETERK971617 · JXG | 510(k) clearances |
| Jun 13, 1997 | PERITONEAL/CARDIAC CATHETERK970983 · JXG | 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
