# Olympus Corporation of the Americas

- Location (FDA's records): Center Valley, PA
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: NWB (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 5 (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
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)

## Firms that cite its devices most
- Olympus Medical Systems Corp.: 2 (https://510kreport.com/company/olympus-medical-systems)
- Ambu A/S: 1 (https://510kreport.com/company/ambu-a-s)
- Guangzhou Red Pine Medical Instrument Co., Ltd.: 1 (https://510kreport.com/company/guangzhou-red-pine-medical-instrument)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)

## Its most-cited devices
- K133538: Visera Cysto-Nephro Videoscope Olympus Cyf Type V2, Visera Cysto-Nephro Videoscope Olympus Cyf Type VA2, Visera Cysto-NE (2014), cited by 5

## Recent decisions
- K133538: Visera Cysto-Nephro Videoscope Olympus Cyf Type V2, Visera Cysto-Nephro Videoscope Olympus Cyf Type VA2, Visera Cysto-NE (Aug 7, 2014)

Source page: https://510kreport.com/company/olympus-of-the-americas