121 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FEEL-DRCS
FDA 510(k)
FDA Class 2
·Radiology
LEONE SPA
FDA UDI
LEONE SPA·08033707096924·BKT 33 INTERACTIVE SL 22 T-11 A+7 BH
OsteoMed
FDA UDI
OSTEOMED LLC·00845694040044·PrimaLIF 3mm Kerrison Rongeur, Forward
Navagio
FDA UDI
Kalitec Direct LLC·B073DRK0100330·Assembly, Navagio Fixed Draw Rod, Large Knob
MTF NEW BONE VOID FILLER
FDA 510(k)
FDA Class 2
·Orthopedic
LIGHT PROJECTOR WITH ENDOSCOPIC CAMERA, 1 CCD CAMERA HEAD NTSC, 1 CCD CAMERA HEAD PAL, LIGHT PROJECTOR, MODEL 5551.107
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PALAXPRESS, CLEAR, 1000G POWDER
FDA Adverse Event
Injury
·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code EBI·February 1, 2012
MG II®
FDA UDI
Zimmer, Inc.·00889024435872·
MG II®
FDA UDI
Zimmer, Inc.·00889024435926·
MG II®
FDA UDI
Zimmer, Inc.·00889024435865·
MG II®
FDA UDI
Zimmer, Inc.·00889024435902·
MG II®
FDA UDI
Zimmer, Inc.·00889024435896·
MG II®
FDA UDI
Zimmer, Inc.·00889024435889·
MG II®
FDA UDI
Zimmer, Inc.·00889024435919·
ICON 25 HCG
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JHI·July 19, 2011
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·JUVEDERM VOLUMA XC
INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019
MAXCEM ELITE
FDA Adverse Event
Malfunction
·KERR CORPORATION·Product code EMA·May 13, 2013
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 23, 2014
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·May 17, 2011