17 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Solar Compact (G4-1)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MaXcess
FDA UDI
Nuvasive, Inc.·00887517195616·MaXcess 4 Removal Tool, Shim Tamp
ADULT TRACHEOSTOMY CLOSED SUCTION SYSTEM 24 HOURS, SIZE 16F
FDA UDI
Intersurgical Incorporated·05030267097845·ADULT TRACHEOSTOMY CLOSED SUCTION SYSTEM 24 HOU...
None
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994318855·LID 6240007 LID ANATOMIC
ARKEO, Wedge Fixation System
FDA UDI
Auxano Medical LLC·00850055649736·ARKEO Wedge Slap Hammer Assy
BARREL REAMER
FDA UDI
Osteocentric Technologies, Inc.·00810189110359·BARREL REAMER
MIRABAY
FDA UDI
Mirabay Orthodontics Corp.·05061075022194·CRIMPABLE STOPS LARGE STAINLESS 0.020-0.019 X 2...
VERIGENE BC-GP NUCLEIC ACID TEST KIT
FDA Adverse Event
Malfunction
·LUMINEX CORPORATION·Product code PAM·July 2, 2024
VERIGENE BC-GP NUCLEIC ACID TEST KIT
FDA Adverse Event
Malfunction
·LUMINEX CORPORATION·Product code PAM·July 2, 2024
INTERFERENTIAL STIMULATOR, MODEL BMLS02-6
FDA 510(k)
FDA Class 2
·Neurology
ABACUS TM SPACER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
4.0 CANN.CANC.BONE SCREW
FDA Adverse Event
Injury
·DEPUY ACE S.A. 'R.L.·Product code HWC·November 19, 2008
OT PING ENHANCED METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·September 8, 2011
DUROM HIP
FDA Adverse Event
Injury
·ZIMER GMBH·Product code KWA·July 18, 2013
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 12, 2026
VERIGENE BC-GP NUCLEIC ACID TEST KIT
FDA Adverse Event
Malfunction
·LUMINEX CORPORATION·Product code PAM·July 24, 2024
VERIGENE BC-GP NUCLEIC ACID TEST KIT
FDA Adverse Event
Malfunction
·LUMINEX CORPORATION·Product code PAM·June 14, 2024