# Leibinger GmbH

- Location (FDA's records): Washington, DC
- FDA decisions: 4 (1994–1997): 4 510(k) clearances
- Names in FDA's records: Leibinger GmbH (3); Leibinger L.P. (1)
- Product codes: IYE (1), DZE (1), LXH (1), HAW (1)
- Predicates its devices cite: 1 (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
- Leibinger & Fischer, Ltd.: 1 (https://510kreport.com/company/leibinger-fischer)

## Firms that cite its devices most
- Tatramed Spol. S.R.O.: 1 (https://510kreport.com/company/tatramed-spol)

## Its most-cited devices
- K946033: Leibinger Stereoplan Plus Sterotactic Treatment Plan Ing Software Package (1995), cited by 1

## Recent decisions
- K954030: Bone-Lock (Nov 14, 1997)
- K946033: Leibinger Stereoplan Plus Sterotactic Treatment Plan Ing Software Package (Sep 1, 1995)
- K944188: Spinal Marker (Apr 13, 1995)
- K924685: STP Complete Module Set and Mask Fixation System (Sep 16, 1994)

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