29 results · 41ms · Sources: EU EUDAMED, US FDA

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EASY-LOAD LENS DELIVERY SYSTEM

FDA 510(k)
FDA Class 1 ·Ophthalmic

AGXO

FDA UDI
Oticon A/S·05707131257802·H150, BTE 13 WL 100 CNB AGXO

Integra®

FDA UDI
INTEGRA PAIN MANAGEMENT·10381780260417·BONE MARROW BIOPSY & ASPIRATION TRAY 11G X 4", ...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166992·Initia Acetabular Standard Liner, E-CIMA 32-48

AUTOSURE VOICE 3 BLOOD GLUCOSE MONITORING SYSTEM AND TEST STRIP

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

THERATEARS CONTACT LENS COMFORT DROPS

FDA 510(k)
FDA Class 2 ·Ophthalmic

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·March 5, 2020

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·March 22, 2020

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 12, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 14, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 11, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 14, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 12, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 12, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 11, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 12, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·March 28, 2020

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·March 28, 2020

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

WIRECUTTER LRG W/CANTILEVER L220

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code FZT·May 29, 2013