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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Raumedic AG with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 29, 2025: NEUROVENT-P (092946-003); NEUROVENT (092956-003); NEUROVENT-IFD-R (095317-003); NEUROVEN….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Aug 29, 2025 | NEUROVENT-P (092946-003); NEUROVENT (092956-003); NEUROVENT-IFD-R (095317-003); NEUROVENT-IFD-S (091678-003); NEUROVENT-P-TEMP (094268-003); NEUROVENT-TEMP (094278-003); NEUROVENT-TEMP-IFD-R (095327-003); NEUROVENT-TEMP-IFD-S (094288-003); NEUROVENT-PTO (095008-003); NEUROVENT-PTO 2L (095108-003); NEUROVENT-PX (091580-003); BOLT-DRILL KIT CH5 (091888-003); BOLT-DRILL KIT CH9 (091898-003); BOLT-DRILL KIT PTO (092380-003); BOLT-DRILL KIT VP 16 (092969-003); BOLT KIT CH5 (091868-003); BOLK250285 · GWM | 510(k) clearances |
| Jul 6, 2017 | MPR2 logO DATALOGGERK171666 · GWM | 510(k) clearances |
| Oct 25, 2013 | RAUMEDIC-PTO-MONITORING-SYSTEMK130529 · GWM | 510(k) clearances |
| Apr 11, 2012 | RAUMEDIC-ICP-TEMP-MONITORING-SYSTEMK120252 · GWM | 510(k) clearances |
| Oct 11, 2011 | RAUMEDIC ICP MONITORING SYSTEMK112017 · GWM | 510(k) clearances |
| Mar 4, 2011 | RAUMEDIC- ICP-MONITORING SYSTEMK103206 · GWM | 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
