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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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19 records meeting your search criteria returned- Product Code: LMH Product Problem: Malposition of Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
GALDERMA Q-MED AB RESTYLANE DEFYNE 06/11/2021
GALDERMA Q-MED AB RESTYLANE DEFYNE 06/11/2021
TEOXANE SA RHA 4 01/05/2021
PROLLENIUM MEDICAL TECHNOLOGIES INC. REVNAESSE VERSA + (WITH LIDOCAINE) 1.0 M 12/04/2020
MERZ NORTH AMERICA RADIESSE+ DERMAL FILLER 12/21/2015
MERZ NORTH AMERICA, INC RADIESSE DERMAL FILLER 09/23/2015
MERZ NORTH AMERICA RADIESSE DERMAL FILLER 07/08/2015
MERZ AESTHETICS, INC RADIESSE DERMAL FILLER 04/29/2015
MERZ AESTHETICS, INC. RADIESSE DERMAL FILLER 04/09/2015
GALDERMA Q-MED SCULPTRA AESTHETIC 04/08/2015
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