24 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TBD
FDA 510(k)
FDA Class 2
·Ophthalmic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526743670·ACHIMED ACHILLES SUPP SILVER IV
ATLANTIS® Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994239938·SCREW 3120214 4.0 X 14 SELF TAP FIX
ATLANTIS® Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000889319·SCREW 3120214 4.0 X 14 SELF TAP FIX
Unity Total Knee System
FDA UDI
CORIN LTD·05056139243530·UNITY KNEE™ PS-C INSERT - Size 2 x 14mm
Cortical Screw, Cannulated
FDA UDI
I.T.S. GmbH·09120069816143·Cortical Screw, Cannulated, D=2.0mm, L=14mm
CRYOPEN CRYOSURGICAL SYSTEM, K102214
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113102·PS Insert, Size 2 x 14mm
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450191286·
General Instrument
FDA UDI
ALPHATEC SPINE, INC.·00840180513668·ALIF, Short Modular Rasped Rotating Distractor,...
CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
MEDIAL ROTATION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDIAL ROTATION KNEE
FDA Adverse Event
Injury
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROATION KNEE
FDA Adverse Event
Malfunction
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROATION KNEE
FDA Adverse Event
Injury
·MATORHTO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROTATION KNEE
FDA Adverse Event
Malfunction
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROTATION KNEE
FDA Adverse Event
Injury
·MATORTHO LIMITED·Product code JWH·January 22, 2016
REFORM PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·PRECISION SPINE, INC·Product code HXX·December 18, 2024
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·Product code OYC·May 20, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 26, 2014