9 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle
FDA 510(k)
FDA Class 2
·Anesthesiology
Oticon
FDA UDI
Oticon A/S·05707131284297·H11V2 TI, BTE 13 WL 85 SGR
AGC TRADITION KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304240841·
NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
OSTEOSYMBIONICS, ST TEMPORALIS IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 6, 2013
ASR ACETABULAR IMPLANT 48
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008
Medical Linear Accelerator
FDA Enforcement
Class II
·Terminated·Elekta, Inc.·September 14, 2016