52 results
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40ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TITANIUM TOGGLE BUTTON(S)
FDA 510(k)
FDA Class 2
·Orthopedic
Baltic Denture System BDLoad
FDA UDI
Merz Dental GmbH·D7091033838·Baltic Denture System BDLoad BDLoad Lw6 PLSEbi...
KSEA CLEARVISION LENS IRRIGATION SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
LUNEAU STERILE TONOMETER SEPARATION PRISMS
FDA 510(k)
FDA Class 2
·Ophthalmic
OPTETRAK
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 2, 2022
LOGIC TIBIA PS MOD INSRT SZ 3 15MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 2, 2022
LOGIC TIBIA PS MOD INSRT SZ 5 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 23, 2022
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·April 3, 2013
UNKNOWN DEPUY ASR HIP
FDA Adverse Event
Injury
·DEPUY INT'L., LTD.·Product code KWA·March 17, 2011
EXETER STEM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CAEN·Product code KWY·April 24, 2008
OPTETRAK
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 4, 2022
LOGIC TIBIA PS MOD INSRT SZ 4 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 3, 2024
NO CODE AVAILABLE
FDA Adverse Event
Injury
·SYNTHES USA·Product code GXN·March 8, 2016
LOGIC TIBIA PS MOD INSRT SZ 5 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 10, 2023
LOGIC TIBIA PS MOD INSRT SZ 5 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 10, 2023
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 11, 2024
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 6, 2025
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 11, 2024
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 9, 2024
LOGIC FEMORAL PS CEM RIGHT SZ 2
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 21, 2024