8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Root ZX3
FDA 510(k)
FDA Class 2
·Dental
TOCO LITE, MODEL TD-01
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
IVAS 20MM (10 GAUGE) BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Orthopedic
LOGIC TIBIA PS MOD INSRT SZ 3 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 19, 2024
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 25, 2014
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 16, 2011
PULSE GEN MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·July 9, 2013
BD ULTRA-FINE¿ MINI PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·January 5, 2022