64 results
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34ms
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Sources: EU EUDAMED, US FDA
VZV IGM TEST
FDA 510(k)
FDA Class 2
·Microbiology
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·G5869113010·round caps, gas or steam permeable, can be used...
FiberFIX
FDA UDI
NANOVA BIO MATERIALS INC·00816537021827·Interference Screw 11x30
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756020381·GUTTER SPLINT
Pinnacle
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730010391·Pinnacle .018 R UR3 -2T 13A 4MO (10PK)
Votion®
FDA UDI
Ortho Organizers, Inc.·00190707114268·Votion .018 R UR3 -2T 13A 4MO (10PK) VOTION
Pinnacle®
FDA UDI
Ortho Organizers, Inc.·00190707112356·Pinnacle .018 R UR3 -2T 13A 4MO (10PK) PINNACLE
Votion
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730008565·Votion .018 R UR3 -2T 13A 4MO (10PK)
INSTINCT JAVA SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Ceribell Pocket EEG Device
FDA 510(k)
FDA Class 2
·Neurology
AUTOSOFT XC
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·July 13, 2024
AUTOSOFT XC
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·July 13, 2024
UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022
5.5MM AGGRESSIVE PLUS CUTTER, FORMULA (5BX)
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY PUERTO RICO·Product code HRX·November 22, 2010
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·January 11, 2013
ECHELON LINEAR CUTTER
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 2, 2014
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code HWC·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 40
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019