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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
SUNRISE MEDICAL (US) LLC QUICKIE Q700M 05/12/2022
PERMOBIL INC. PERMOBIL F3 CORPUS 02/08/2022
HOVEROUND CORPORATION HOVEROUND 01/21/2022
HOVEROUND CORPORATION HOVEROUND 01/06/2022
ALBER GMBH SMOOV O10 12/08/2021
HOVEROUND CORPORATION HOVEROUND 10/20/2021
HOVEROUND CORPORATION HOVEROUND 10/20/2021
PERMOBIL INC. PERMOBIL M3 10/08/2021
MAX MOBILITY LLC SMARTDRIVE 09/28/2021
PERMOBIL INC. PERMOBIL F3 CORPUS 09/02/2021
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