29 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CLYDESDALES SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017705·K-Wire, Double Ended, Trocar Point, Diameter Si...
2540 BALLOON VALVE
FDA UDI
HANS RUDOLPH, INC.·00874750008735·2540C 4WAYTSHP INFLBAL 1.375OD
AOS TIBIAL NAIL 12mm x 40.5cm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016369·
TLIF/PLIF Disc Prep
FDA UDI
Life Spine, Inc.·00190837086817·
Vu CPOD™
FDA UDI
Seaspine Orthopedics Corporation·10889981052034·Implant Tapered 12x14x5mm (Strut)
INFUSION SET FOR POWERPICC SOLO 2 CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
EXTRUDE MODIFIED
FDA 510(k)
FDA Class 2
·Dental
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·April 18, 2022
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·May 14, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 24, 2014
FLEXICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·June 3, 2011
UNKNOWN GUIDE WIRE
FDA Adverse Event
Malfunction
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·February 21, 2023
ZNN¿, CMN LAG SCREW, Ø 10.5 MM, 95 MM INCLUDING SET SCREW
FDA Adverse Event
Malfunction
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·February 21, 2023
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 19, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·January 16, 2023
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·December 19, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·December 19, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 7, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·December 13, 2022