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 14, 2026, FDA's public records list Stockert GmbH with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 14, 2007: STOCKERT NEURO N50, MODEL12267.
| Jun 14, 2007 | STOCKERT NEURO N50, MODEL12267K070336 · GXD | 510(k) clearances |
| Mar 22, 2007 | MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098K070134 · BXN | 510(k) clearances |
| Nov 21, 2006 | STIMUPLEX PENK061983 · BXN | 510(k) clearances |
| Nov 17, 2005 | STIMUPLEX HNS-12, MODEL 4892098K052313 · BXN | 510(k) clearances |
| Jun 6, 2001 | STIMUPLEX HNS-11K003983 · BXN | 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
