13 results
·
19ms
·
Sources: EU EUDAMED, US FDA
VACUUM STRETCHER IMMOBILIZER
FDA 510(k)
FDA Class 1
·General Hospital
Kinetic Dynamic Anterior Cervical Plate System
FDA UDI
Life Spine, Inc.·00190837004811·
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591013400·Adjustable Elbow Brace, Right
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591013394·Adjustable Elbow Brace, Left
NA
FDA UDI
Zimmer, Inc.·00889024101968·
BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER
FDA 510(k)
FDA Class 2
·Orthopedic
SUREFIRE GUIDING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
Zimmer, Inc.·00889024074002·
DREAMSTATION AUTO BIPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·January 27, 2023
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014
SCREW
FDA Adverse Event
Injury
·SYNTHES·Product code HWC·November 20, 2012
ACRYSOF IQ TORIC
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·September 15, 2010
KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and cold packs that can be interchanged depending on the therapy type desired
FDA Recall
Terminated
·KT Health, LLC·Product code IME·September 16, 2019