# Cybersonics, Inc.

- Location (FDA's records): Erie, PA
- FDA decisions: 7 (2005–2017): 7 510(k) clearances
- Product codes: FFK (5), FEO (2)
- Predicates its devices cite: 9 (7 its own); citations of its devices by later devices: 9 (7 its own)
- Recalls linked to its devices: 8 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Electro Medical Systems SA: 1 (https://510kreport.com/company/electro-medical-systems)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)

## Firms that cite its devices most
- Med-Sonics Corp.: 2 (https://510kreport.com/company/med-sonics)

## Its most-cited devices
- K052135: Cybersonics Cyberwand Dual Probe Lithotripter (2005), cited by 3
- K102169: Cyberwand Lithotripter (2010), cited by 2
- K120303: Cyberwand Dual Action Ultrasonic Lithotripsy System (2012), cited by 2
- K142428: Shock Pulse-SE Lithotripsy System CYBERWAND II (2014), cited by 1
- K072422: Cyberwand Sterile Pads, Model: CW-Rbpbx (2007), cited by 1

## Recent decisions
- K171024: ShockPulse-SE Lithotripsy System (Aug 21, 2017)
- K142428: Shock Pulse-SE Lithotripsy System CYBERWAND II (Nov 13, 2014)
- K132795: Cyberwand Sterile Probe Set (Nov 26, 2013)
- K120303: Cyberwand Dual Action Ultrasonic Lithotripsy System (Jun 5, 2012)
- K102169: Cyberwand Lithotripter (Aug 30, 2010)
- K072422: Cyberwand Sterile Pads, Model: CW-Rbpbx (Oct 24, 2007)
- K052135: Cybersonics Cyberwand Dual Probe Lithotripter (Dec 20, 2005)

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