59 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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uWS-MI
FDA 510(k)
FDA Class 2
·Radiology
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741926300·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674192630060·
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180544792·Sigma Cervical Blade, Narrow, Thin, Teeth, 30mm
IN:C2 SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ZIROX
FDA 510(k)
FDA Class 2
·Dental
INTELLAMAP ORION?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·May 12, 2026
INTELLAMAP ORION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 15, 2025
INTELLAMAP ORION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 29, 2026
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 22, 2014
USS-II POLYAX SCRHOLDER3
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LXH·June 27, 2013
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·July 1, 2011
INTELLAMAP ORION?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 17, 2026
INTELLAMAP ORION?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·January 30, 2026
INTELLAMAP ORION?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 1, 2026
INTELLAMAP ORION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·November 21, 2024
CMK OC - RASP S303
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·January 28, 2026
INTELLAMAP ORION?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DRF·February 26, 2026
CMK OC - RASP S303
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·January 28, 2026
CMK OC - RASP S202
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·February 5, 2026