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ULTRAMAT S
SDI LIMITED · Model 5546057 · UDI-DI 09336472005535
10
510(k) clearances
6
Adverse events
1
Recalls
32
Facilities
Description
ULTRAMAT S US
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-20 | SDI Limited | Potential for electrical discharge from unit when unplugged. |
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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.