# Stockert GmbH

- Location (FDA's records): Freiburg, B-W, DE
- FDA decisions: 5 (2001–2007): 5 510(k) clearances
- Product codes: BXN (4), GXD (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 6 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Hdc Corp.: 1 (https://510kreport.com/company/hdc)
- Leibinger & Fischer, Ltd.: 1 (https://510kreport.com/company/leibinger-fischer)

## Firms that cite its devices most
- Xavant Technology (Pty), Ltd.: 2 (https://510kreport.com/company/xavant-technology)
- Neurometrix, Inc.: 1 (https://510kreport.com/company/neurometrix)
- Relievant Medsystems: 1 (https://510kreport.com/company/relievant-medsystems)

## Its most-cited devices
- K052313: Stimuplex HNS-12, Model 4892098 (2005), cited by 4
- K003983: Stimuplex HNS-11 (2001), cited by 1
- K070336: Stockert Neuro N50, MODEL12267 (2007), cited by 1

## Recent decisions
- K070336: Stockert Neuro N50, MODEL12267 (Jun 14, 2007)
- K070134: Modification to Stimuplex HNS-12, Model 4892098 (Mar 22, 2007)
- K061983: Stimuplex Pen (Nov 21, 2006)
- K052313: Stimuplex HNS-12, Model 4892098 (Nov 17, 2005)
- K003983: Stimuplex HNS-11 (Jun 6, 2001)

Source page: https://510kreport.com/company/stockert