# Karl Storz Lithotripsy-America, Inc.

- Location (FDA's records): Culver City, CA
- FDA decisions: 1 (2001–2001): 1 510(k) clearance
- Product codes: LNS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Direx Systems Corp.: 2 (https://510kreport.com/company/direx-systems)
- E.S.W.L. Products, Inc.: 1 (https://510kreport.com/company/eswl-products)
- United Medical Systems, Inc.: 1 (https://510kreport.com/company/united-medical-systems)

## Its most-cited devices
- K010340: Modulith Lithotripsy, Model SLK for the Fragmentation of Urinary and Upper Ureteral Calculi (2001), cited by 4

## Recent decisions
- K010340: Modulith Lithotripsy, Model SLK for the Fragmentation of Urinary and Upper Ureteral Calculi (Feb 13, 2001)

Source page: https://510kreport.com/company/karl-storz-lithotripsy-america