130 results · 23ms · Sources: EU EUDAMED, 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