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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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174 records meeting your search criteria returned- Product Code: ITI Product Problem: Use of Device Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
HOVEROUND CORPORATION HOVEROUND 09/01/2021
PERMOBIL INC. PERMOBIL M300 08/25/2021
SUNRISE MEDICAL (US) LLC QUICKIE PULSE 08/25/2021
SUNRISE MEDICAL (US) LLC QUICKIE 08/13/2021
HOVEROUND CORPORATION HOVEROUND 08/12/2021
SUNRISE MEDICAL (US) LLC QUICKIE 07/24/2021
HOVEROUND CORPORATION HOVEROUND 07/16/2021
HOVEROUND CORPORATION HOVEROUND 05/26/2021
ALBER GMBH E-MOTION M15 04/26/2021
PERMOBIL AB (PAB) F5 CORPUS VS 04/12/2021
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