17 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LINK MP Monoblock Hip Prosthesis
FDA 510(k)
FDA Class 2
·Orthopedic
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515027916·Skin Ret, cross act, 4x4 prngs, 4" sharp
LINK Instrument
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575180523·Trial Insert
I-STAT EC8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·March 20, 2019
LOW ADHERENT AFM AG DRESSINGS
FDA 510(k)
FDA Unclassified
·Unknown
SIMPACT ENDOSSEOUS DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code ITI·June 21, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 28, 2011
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·October 17, 2014
UNKNOWN JOINT REPAIR DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026
UNKNOWN JOINT REPAIR DEVICE
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026
UNKN JOINT REPAIR DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026
UNKNOWN
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026
UNKNOWN JOINT REPAIR DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026
UNKNOWN JOINT REPAIR DEVICE
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026
UNKN JOINT REPAIR DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026
UNKN JOINT REPAIR DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026