Home › Device types › LNS
Lithotriptor, Extracorporeal Shock-Wave, Urological
FDA product code LNS · Class 2 · Gastroenterology, Urology
131
Registered devices
811
Adverse events
1
Recalls
56
510(k) clearances
Devices with this code
PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCMODULITH® — Storz Medical AGDornier MedTech — Dornier MedTech GmbHPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.Extracorporeal Shock Wave Lithotripter — Suzhou Xixin Medical Instruments Co., Ltd.Sonolith i-move Standard Module — EDAP-TMS FRANCEPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.Econolith EM1000 — MEDISPEC LTD.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCModularis Variostar — Siemens Healthcare GmbHEconolith EM1000 — MEDISPEC LTD.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-09-24 | Siemens Medical Solutions USA, Inc | Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.