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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. GII SPC REAMTHRU CR TR SZ 6 LT 01/14/2021
SMITH & NEPHEW, INC. GII SLT 3 MOD TIB CUTBLCK RT 12/30/2020
SMITH & NEPHEW, INC. GII SLT 3 MOD TIB CUTBLCK LT 12/30/2020
SMITH & NEPHEW, INC. GII DCF VARIABLE SZ GUIDE RT 12/18/2020
SMITH & NEPHEW, INC. GII SPC PRI SPACER BLOCK 12/16/2020
SMITH & NEPHEW, INC. EXPRESS INSTRUMENT JOURNEY PROJECT 12/10/2020
SMITH & NEPHEW, INC. GII MIS DCF ALIGN GDE 12/03/2020
DEPUY ORTHOPAEDICS INC US DURALOC MARATHON 10D 28 FOCUSED LINER 4 12/02/2020
SMITH & NEPHEW, INC. GII MI IN SLT 3 MO TI CU BL RT 11/27/2020
SMITH & NEPHEW, INC. CORKSCREW FEM HEAD REMOVER 11/26/2020
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