# Leibinger & Fischer, Ltd.

- Location (FDA's records): Dallas, TX
- FDA decisions: 2 (1990–1991): 2 510(k) clearances
- Product codes: IYE (1), GXD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (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 that cite its devices most
- Stryker Instruments: 1 (https://510kreport.com/company/stryker-instruments)
- Medical Instrumentation & Diagnostics Corp.(Midco): 1 (https://510kreport.com/company/medical-instrumentation-diagnostics-midco)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Leibinger GmbH: 1 (https://510kreport.com/company/leibinger)
- Howmedica Leibinger, Inc.: 1 (https://510kreport.com/company/howmedica-leibinger)
- Stockert GmbH: 1 (https://510kreport.com/company/stockert)
- Elekta Instrument AB: 1 (https://510kreport.com/company/elekta-instrument)
- Howmedica Corp.: 1 (https://510kreport.com/company/howmedica)

## Its most-cited devices
- K892425: STP Complete Module Set (1990), cited by 6
- K896450: Neuro N 50 Lesion Generator (1991), cited by 2

## Recent decisions
- K896450: Neuro N 50 Lesion Generator (Mar 19, 1991)
- K892425: STP Complete Module Set (Mar 23, 1990)

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