130 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MAS TOX CONTROL
FDA 510(k)
FDA Class 1
·Clinical Toxicology
n/a
FDA UDI
Ortho Development Corporation·00822409075119·Distal Reamer 8.5mm
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014604428·SHAMPAINE 4900 2.25"SOFTCARE PLUS FOAM W/ SOFTC...
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 85mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665025101·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450180136·
Mariner Cortical
FDA UDI
Seaspine Orthopedics Corporation·10889981166687·CORTICAL SHANK, SOLID, 8.0 X 85
Mariner Cortical
FDA UDI
Seaspine Orthopedics Corporation·10889987166681·CORTICAL SHANK, SOLID, 8.0 X 85
PORTSETT
FDA 510(k)
FDA Class 2
·General Hospital
EEG REAL PATIENT SPIKE AND EVENT DETECTOR MODULE, MODEL EX-SP-RP (PROPOSED)
FDA 510(k)
FDA Class 2
·Neurology
Apelo® / Apelo® MIS
FDA UDI
ATLAS SPINE, INC.·M68111000800850·5.5mm x 85mm Straight Secure Rod
CARDIOSAVE RESCUE, 3.1 EDITION
FDA UDI
Datascope Corp.·10607567113449·CARDIOSAVE RESCUE, 3.1 EDITION
COCR FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·July 23, 2025
WAVEWRITER ALPHA? PRIME
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 29, 2025
MASTERLOC CEMENTLESS TI COATED STD STEM SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·May 29, 2018
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·April 26, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·April 6, 2011
NATURAL-KNEE II SYSTEM DURASUL ULTRACONGRUENT TIBIAL INSERT
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code HSH·July 17, 2008
LINER: MPACT FLAT PE HC 36/E
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·May 5, 2021
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019