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Lithotriptor, Extracorporeal Shock-Wave, Urological

FDA product code LNS · Class 2 · Gastroenterology, Urology

131
Registered devices
818
Adverse events
1
Recalls
56
510(k) clearances

Devices with this code

Econolith EM1000 — MEDISPEC LTD.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 SERVICE SOLUTIONS, LLCMODULITH® — Storz Medical AGPIEZOLITH 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 SERVICE SOLUTIONS, LLCPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.MODULITH® — Storz Medical AGPIEZOLITH 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, LLCINTEGRA — DIREX SYSTEMS CORP.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.Dornier MedTech — Dornier MedTech GmbHPIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED MEDICAL SYSTEMS (DE), INC.PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPSY SYSTEM COMPLETE — UNITED SERVICE SOLUTIONS, LLCCOMPACT DUET — DIREX SYSTEMS CORP.

Recent recalls

DateFirmReason
2015-09-24Siemens Medical Solutions USA, IncDisplay freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.

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