# Baitella AG

- Location (FDA's records): Amsterdam, Nh, NL
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: GCJ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (0 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
- KLS-Martin L.P.: 1 (https://510kreport.com/company/kls-martin)
- Integra Neurocare, LLC: 1 (https://510kreport.com/company/integra-neurocare)
- Omni-Tract Surgical, Div. Minn. Scientific, Inc.: 1 (https://510kreport.com/company/omni-tract-surgical-div-minn-scientific)

## Firms that cite its devices most
- Surgical Innovations Group Plc: 1 (https://510kreport.com/company/surgical-innovations-group)
- Biomet Microfixation: 1 (https://510kreport.com/company/biomet-microfixation)

## Its most-cited devices
- K070509: Fisso Holding System (2007), cited by 2

## Recent decisions
- K070509: Fisso Holding System (Mar 22, 2007)

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