23 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SECULOK ACP System
FDA 510(k)
FDA Class 2
·Orthopedic
Oticon
FDA UDI
Oticon A/S·05707131340870·G500 FW 6.0
Pre-Finisher
FDA UDI
TP ORTHODONTICS INC·00192029041550·Non-Extraction
N/A
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055001·MTM® NO TRACE (TM) 018 UL/4-4
IN-OVATION® L
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055011·IN-OVATION® L 018 UPPER 6-6
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws
IN-OVATION® L
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055101·IN-OVATION® L 018 UL/7-7
MATTIOLI PULSE TWO/THREE PLUS FAMILY
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
APTUS 2.0 RADIAL HEAD SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BD PEN NDL 31GA 8MM
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·September 17, 2021
SOF-FLEX MULTI-LENGTH URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·October 24, 2024
G7 NEUTRAL E1 LINER 36MM D
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code PBI·February 28, 2018
2.4MM TI LOCKING SCREW 12MM F/LOCKING RECONSTRUCTION PLATE
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HWC·October 6, 2008
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013
ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FRN·June 29, 2011
SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·September 30, 2024
SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·October 7, 2024
SOF-FLEX MULTI-LENGTH URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·October 21, 2024
SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·April 19, 2021
SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·April 19, 2021