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MODULITH®
Storz Medical AG · Model SLX-F2 · UDI-DI 07630039101459
LNS
Prescription
2
510(k) clearances
811
Adverse events (30 deaths)
1
Recalls
18
Facilities
Description
Equipment for the extracorporeal induced shock wave therapy for stationary and mobile use.
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. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
