30 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SECURMARK BIOPSY SITE MARKING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GoLIF! Lumbar Interbody Fusion System
FDA UDI
GetSet Surgical SA·07640387660348·GoLIF! Lumbar Interbody Fusion Device, 1 PEEK p...
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699427·GENUMEDI SILVER SIZE VIII
Carbide burs
FDA UDI
DFS - DIAMON GmbH·04057176153074·Carbide 2 FG 0,8 mm
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383556828·Gutta Percha Points is used to root canal filin...
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383502788·Gutta Percha Points is used to root canal filin...
InFill Contour TLIF
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729025301·
PLATEAU-TL
FDA UDI
Life Spine, Inc.·00190837028329·PLATEAU-TL Interbody, Convex, Bulleted, 10mm x ...
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837026202·PLATEAU Interbody, Straight, Bulleted, 10mm 26m...
INVAC
FDA 510(k)
FDA Class 2
·Radiology
BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS-ENCODE ABUTMENTS
FDA 510(k)
FDA Class 2
·Dental
INFINION CX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 5, 2023
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785913·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785340·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785838·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785449·
MANUAL ORTHOPEDIC SURGICAL INSTRUMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·May 9, 2013
VENTRIO MESH
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·September 11, 2014
INRATIO2
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO INC.·Product code GJS·May 20, 2011