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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 340MM SHAFT 01/12/2024
COVIDIEN LP LLC NORTH HAVEN TRI-STAPLE 2.0 01/12/2024
DAVOL INC., SUB. C.R. BARD, INC. -121364 SORBAFIX ENHANCED 01/12/2024
DAVOL INC., SUB. C.R. BARD, INC. -121364 SORBAFIX ENHANCED 01/12/2024
DAVOL INC., SUB. C.R. BARD, INC. -121364 SORBAFIX ENHANCED 01/12/2024
US SURGICAL PUERTO RICO GIA 01/11/2024
US SURGICAL PUERTO RICO ENDO GIA ULTRA 01/11/2024
ETHICON ENDO-SURGERY, LLC. POWERED PLUS STANDARD 45 01/11/2024
COVIDIEN LP LLC NORTH HAVEN UNKNOWN ENDO GIA SULU 01/10/2024
DAVIS & GECK CARIBE LTD UNKNOWN VLOC ENDO STITCH RELOAD ABS 01/09/2024
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