# Od-Os GmbH

- Location (FDA's records): Laguna Beach, CA
- FDA decisions: 4 (2009–2025): 4 510(k) clearances
- Product codes: HQF (2), GEX (2)
- Predicates its devices cite: 13 (3 its own); citations of its devices by later devices: 3 (3 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
- Topcon Medical Laser Systems, Inc.: 2 (https://510kreport.com/company/topcon-medical-laser-systems)
- Iridex Corp: 2 (https://510kreport.com/company/iridex)
- Meridian AG: 1 (https://510kreport.com/company/meridian)
- Opto Global, Inc.: 1 (https://510kreport.com/company/opto-global)
- Carl Zeiss Meditec, AG: 1 (https://510kreport.com/company/carl-zeiss-meditec)
- Carl Zeiss Jena GmbH: 1 (https://510kreport.com/company/carl-zeiss-jena)
- Nidek, Inc.: 1 (https://510kreport.com/company/nidek)
- Quantel Medical: 1 (https://510kreport.com/company/quantel-medical)

## Its most-cited devices
- K091064: Navilas Laser System (2009), cited by 1
- K162191: NAVILAS Laser System (2016), cited by 1
- K141851: Navilas Laser System (2015), cited by 1

## Recent decisions
- K251772: Navilas Laser System 577sl (156691) (Oct 29, 2025)
- K162191: NAVILAS Laser System (Nov 22, 2016)
- K141851: Navilas Laser System (Jan 2, 2015)
- K091064: Navilas Laser System (Oct 27, 2009)

Source page: https://510kreport.com/company/od-os