44 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDICULT VITRIFICATION COOLING/WARMING, MODEL REF: 1228, 1229
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Bur PM2-70 80K Diam Ø1.0 St
FDA UDI
Bien-Air Surgery SA·17630055503333·
Bur PM2-70 80K diamond Ø1.0mm sterile
FDA UDI
Bien-Air Surgery SA·J00711003670011·
Tether™
FDA UDI
Seaspine Orthopedics Corporation·10889981035686·Plate - 3 Level - 67mm
Reison
FDA UDI
Stille AB·07332339229825·Tibia Support Short
SECURMIX
FDA 510(k)
FDA Class 2
·General Hospital
MODIFICATION TO TITANIUM TRI-LOCK HIPS STEM
FDA 510(k)
FDA Class 2
·Orthopedic
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 6, 2015
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 20, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 26, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 11, 2016
FLANGE FIXTURE ST 4MM W. BAHA ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 11, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·July 21, 2016
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·May 31, 2016
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
SP MAGNET 3
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 13, 2016
BIA400 IMPLANT 4MM W ABUTMENT 10MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 5, 2015
PINNACLE 300 ACET CUP 54MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·May 8, 2013
G4 PLATINUM PEDIATRIC CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·September 18, 2014