36 results · 24ms · Sources: EU EUDAMED, US FDA

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Visaris Vision® (Vision C, Vision U. Vision V, Vision X)

FDA 510(k)
FDA Class 2 ·Radiology

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017873·K-Wire, Double Ended, Trocar Point, Diameter 0....

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017866·K-Wire, Double Ended, Trocar Point, Diameter Si...

Responsive Orthopedics Total Knee Arthroplasty System

FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973106708·TRIAL 90-SRK-160620 POLY CR 6X20MM

B-P TOTAL HIP SYSTEM

FDA UDI
ENDOTEC, INC.·00814193024510·B-P MODULAR EXTENSION W/ULTRACOAT - 20 MM X 150 MM

ACCU-CHEK AVIVA TEST STRIPS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR , MODEL KN-550

FDA 510(k)
FDA Class 2 ·Cardiovascular

BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 8, 2021

Widex

FDA UDI
Widex A/S·05706069975222·WIDEX MOMENT M-CIC-M (TR) 220 (Light beige)

Widex

FDA UDI
Widex A/S·05706069815375·Widex UNIQUE U-CIC-M TR (Light beige ) 220, Tra...

Widex

FDA UDI
Widex A/S·05706069975246·WIDEX MOMENT M-CIC-M (TR) 220 (Dark brown)

Widex

FDA UDI
Widex A/S·05706069815382·Widex UNIQUE U-CIC-M TR (Clay brown ) 220, Tran...

Widex

FDA UDI
Widex A/S·05706069975239·WIDEX MOMENT M-CIC-M (TR) 220 (Clay brown)

Widex

FDA UDI
Widex A/S·05706069815399·Widex UNIQUE U-CIC-M TR (Dark brown ) 220, Tran...

BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)

FDA Adverse Event
Injury ·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 11, 2021

BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·September 27, 2021

MAGEC RODS

FDA Adverse Event
Malfunction ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC·Product code PGN·October 8, 2019

COBAS INTEGRA 800

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 5, 2017

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
UNKNOWN·Product code IKX·June 10, 2013

LIBERTY CYCLER SET, SET, SINGLE CONN./EXT. D

FDA Adverse Event
Injury ·REYNOSA MANUFACTURING·Product code FKX·July 6, 2011