157 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Biograph Vision
FDA 510(k)
FDA Class 2
·Radiology
LEONE SPA
FDA UDI
LEONE SPA·08033707069478·HOW PLIERS CURVED
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101056·KNAPP RETRACTOR 4-PRONG BLUNT
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702385618·Elvarex Forte 3/Thigh High/Slant-Open Toe-Eleph...
Remedy
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215008048·
OrthoMedFlex, LLC
FDA UDI
ORTHOMEDFLEX LLC·M7161111909000·Orion Stem, Standard Offset, Size 9
Paxeon Remedy
FDA UDI
PAXEON RECONSTRUCTION LLC·08177570201143·Remedy Stem Size 9 Standard Offset
Remedy Hip Stem
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215053178·
MOTIVATION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ADVIA CHEMISTRY DRUG CALIBRATOR II, MODEL 10376771
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SKYLON Stem
FDA UDI
AMPLITUDE SAS·03701089520409·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024495548·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024495555·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024495562·
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 21, 2014
EON MINI RECHARGEABLE IPG
FDA Adverse Event
Malfunction
·ST JUDE MED - NEUROMODULATION·Product code LGW·July 19, 2011
PAINSMART
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·June 14, 2013
BD PANEL PHOENIX NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 18, 2024
BD PANEL PHOENIX NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 2, 2024
BD PHOENIX PANEL NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025