25 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEMOSIL PROTEIN C
FDA 510(k)
FDA Class 2
·Hematology
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X0624300·6mm H x 24mm W x 30mm L x 0 degrees XLIF
OsteoMed
FDA UDI
OSTEOMED LLC·00845694008457·2.4mm x 30mm Lag Screw
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X06243080·6mm H x 24mm W x 30mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L062430120·6mm H x 24mm W x 30mm L XLIF Trial 12 degree Lo...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X062430120·6mm H x 24mm W x 30mm L x 12 degrees XLIF
OsteoMed
FDA UDI
OSTEOMED LLC·00845694035187·2.4 x 30mm Lag Screw, Sterile
OsteoMed
FDA UDI
OSTEOMED LLC·00845694067089·HPS 2.4 x 30mm Lag Screw Sterile Qty 5
MULTI-METER GLUCOSE CALIBRATION VERIFICATION MATERIAL, MODEL RNA GL3
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ISO FUNCTIONAL
FDA 510(k)
FDA Class 2
·Dental
SOL-MILLENNIUM
FDA Adverse Event
Malfunction
·SOL-MILLENNIUM MEDICAL INC·Product code FMF·May 16, 2025
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 16, 2013
RUSCH ENDOTRACHEAL TUBE AGT ORAL CUFFED 7.5MM
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTR·March 18, 2011
S5
FDA Adverse Event
Malfunction
·SORIN GROUP, USA, INC.·Product code DTQ·May 31, 2008
S-ROM M HEAD 36MM +0
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 21, 2012
PINNACLE MTL INS NEUT36IDX60OD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 21, 2012
S-ROM M HEAD 36MM +0
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 21, 2012
PINNACLE MTL INS NEUT36IDX60OD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 21, 2012
PINNACLE SECTOR II CUP 60MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 26, 2013
PINN CAN BONE SCREW 6.5MMX45MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code NDJ·August 26, 2013