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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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409 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
ALLERGAN (PRINGY) UNK VOLBELLA 02/07/2022
ALLERGAN (PRINGY) JUVEDERM VOLLURE XC 2X1 ML 02/01/2022
MERZ NORTH AMERICA, INC RADIESSE (+) INJECTABLE IMPLANT 01/26/2022
ALLERGAN (PRINGY) JUVEDERM VOLUMA XC/LIDO (VOLUME UNKNOWN) 01/24/2022
TEOXANE RHA4 01/21/2022
MERZ NORTH AMERICA, INC RADIESSE INJECTABLE IMPLANT 01/20/2022
ALLERGAN (PRINGY) JUVEDERM VOLLURE XC 2X1 ML 01/20/2022
ALLERGAN (PRINGY) JUVEDERM ULTRA PLUS/30HV (VOLUME UNKNOWN 01/19/2022
Q-MED RESTYLANE CONTOUR 01/18/2022
Q-MED RESTYLANE CONTOUR 01/18/2022
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