# Stockert Instrumente GmbH

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 9 (2001–2004): 9 510(k) clearances
- Product codes: DWA (3), DWF (3), DTQ (2), DTW (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 5 (1 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Stoeckert Instrumente: 3 (https://510kreport.com/company/stoeckert-instrumente)
- Jostra Medizintechnik AG: 2 (https://510kreport.com/company/jostra-medizintechnik)
- Himex Production Corp.: 1 (https://510kreport.com/company/himex-production)
- Rocky Mountain Research, Inc.: 1 (https://510kreport.com/company/rocky-mountain-research)

## Firms that cite its devices most
- Sorin Group Deutschland GmbH: 2 (https://510kreport.com/company/sorin-group-deutschland)
- Cardiovention, Inc.: 1 (https://510kreport.com/company/cardiovention)
- Spectrum Medical, Ltd.: 1 (https://510kreport.com/company/spectrum-medical)

## Its most-cited devices
- K011838: Centrifugal Pump (2002), cited by 3
- K041558: Stockertir Purge Control (Apc) System (2004), cited by 1
- K042374: Stockert SCP Rhythm (2004), cited by 1

## Recent decisions
- K042374: Stockert SCP Rhythm (Sep 23, 2004)
- K041558: Stockertir Purge Control (Apc) System (Jul 2, 2004)
- K032213: Stockert Centrifugal Pump System with Tubing Clamp (Aug 29, 2003)
- K023622: Stockert Pediatric Aortic Cannulae, Model Numbers A272-15 Through A272-35 (Nov 21, 2002)
- K022280: Stockert Coronary Perfusion Cannulae (Oct 11, 2002)
- K022321: Stockert V172-28 Venous Femoral Cannula (Oct 9, 2002)
- K020571: Stockert Centrifugal Pump Console (Sep 23, 2002)
- K011838: Centrifugal Pump (Feb 5, 2002)

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