# K2 Medical GmbH & Co. KG

- Location (FDA's records): Tuttlingen, DE
- FDA decisions: 2 (2012–2016): 2 510(k) clearances
- Product codes: HAE (1), DXC (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- Instrumed International, Inc.: 2 (https://510kreport.com/company/instrumed-international)
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)

## Firms that cite its devices most
- KLS-Martin L.P.: 1 (https://510kreport.com/company/kls-martin)

## Its most-cited devices
- K150468: Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs (2016), cited by 1

## Recent decisions
- K150468: Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs (Feb 29, 2016)
- K120492: K2 Medical Vascular Clamps (Apr 30, 2012)

Source page: https://510kreport.com/company/k2-medical