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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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100 records meeting your search criteria returned- Product Code: LMH Patient Problem: Foreign Body Reaction Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
GALDERMA Q-MED UNSPECIFIED HA FILLER 12/10/2018
GALDERMA Q-MED RESTYLANE REFYNE 11/07/2018
GALDERMA Q-MED RESTYLANE LYFT WITH LIDOCAINE 11/07/2018
GALDERMA Q-MED RESTYLANE REFYNE 11/07/2018
GALDERMA Q-MED SCULPTRA AESTHETIC 10/26/2018
MERZ NORTH AMERICA, INC. RADIESSE(+) INJECTABLE IMPLANT 08/29/2018
ALLERGAN (PRINGY) JUVEDERM ULTRA PLUS XC 1 ML ROW 06/07/2018
GALDERMA Q-MED UNSPECIFIED HA FILLER 05/10/2018
ANTEIS S.A. HYALURONIC ACID 05/09/2018
SUNEVA MEDICAL, INC. ARTEFILL - NOW BELLAFILL 04/26/2018
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