# Schwind Eye-Tech-Solutions GmbH & Co. KG

- Location (FDA's records): Coto De Caza, CA
- FDA decisions: 2 (2004–2008): 2 510(k) clearances
- Product codes: HNO (2)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 3 (1 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
- Moria SA: 1 (https://510kreport.com/company/moria)
- Chiron Vision Corp.: 1 (https://510kreport.com/company/chiron-vision)
- Plancon Instruments: 1 (https://510kreport.com/company/plancon-instruments)
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)
- Lasersight Technologies, Inc.: 1 (https://510kreport.com/company/lasersight-technologies)
- Biovision, Inc.: 1 (https://510kreport.com/company/biovision)
- Becton, Dickinson & CO: 1 (https://510kreport.com/company/becton-dickinson)
- Intra Lase Corp.: 1 (https://510kreport.com/company/intra-lase)

## Firms that cite its devices most
- Intra Lase Corp.: 1 (https://510kreport.com/company/intra-lase)
- Alcon Research, Ltd.: 1 (https://510kreport.com/company/alcon-research)

## Its most-cited devices
- K032910: Carriazo Pendular (2004), cited by 3

## Recent decisions
- K082043: Carriazo-Pendular Microkeratome (Aug 1, 2008)
- K032910: Carriazo Pendular (Aug 30, 2004)

Source page: https://510kreport.com/company/schwind-eye-tech-solutions
