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iotaSOFT Insertion System
Iotamotion, Inc. · Model IM-05 · UDI-DI 00850002960068
QQH
Prescription
1
510(k) clearances
11
Adverse events
1
Recalls
4
Facilities
Description
iotaSOFT Plus Drive Unit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-09-12 | Iotamotion Inc | Incorrect GTIN number. |
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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.