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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
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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451 records meeting your search criteria returned- Product Code: LMH Patient Problem: Obstruction/Occlusion Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
MERZ NORTH AMERICA, INC RADIESSE(+) INJECTABLE IMPLANT 06/14/2022
Q-MED RESTYLANE DEFYNE 06/08/2022
Q-MED RESTYLANE DEFYNE 06/08/2022
ALLERGAN (PRINGY) JUVEDERM VOLUMA (VOLUME/ADDITIVE UNKNOWN 06/02/2022
ALLERGAN (PRINGY) VOLIFT (VOLUME UNKNOWN) 06/02/2022
ALLERGAN (PRINGY) JUVEDERM VOLBELLA XC 2 X 1ML 32G 06/01/2022
ALLERGAN (PRINGY) JUVEDERM VOLIFT W/LIDO 2X1ML EAME SKU1 05/26/2022
ALLERGAN (PRINGY) JUVEDERM ULTRA XC (1 ML COC) 05/26/2022
ALLERGAN (PRINGY) JUVEDERM VOLLURE XC 2X1 ML 05/25/2022
UNKNOWN MANUFACTURER UNK DERMAL FILLER 05/25/2022
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