2,598 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GALLERY LAMINOPLASTY FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814565·GENUMEDI SAND SIZE V
Bur PM2-70 80K Acorn Ø6.0 St
FDA UDI
Bien-Air Surgery SA·17630055512793·
Turbo Wire
FDA UDI
ORMCO CORPORATION·00889989027327·TURBO ARCH UPPER 21 X25 PACK/10
Biliary Drainage Tube
FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170046360·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450489161·
PRISMA SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
KAVO K.E.Y. LASER 1242
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Widex
FDA UDI
Widex A/S·05706069725049·Widex EVOKE E-XP (Light beige S-110 ) Telecoil,...
Widex
FDA UDI
Widex A/S·05706069722918·Widex UNIQUE U-XP ITE (Light beige S-110 ) Tele...
Widex
FDA UDI
Widex A/S·05706069724684·Widex D-CIC (Light beige S-110 ) Right, RC coil
Widex
FDA UDI
Widex A/S·05706069723397·Widex D-XP ITE (Light beige S-110 ) Telecoil, R...
Widex
FDA UDI
Widex A/S·05706069724325·Widex UNIQUE U-CIC (Light beige S-110 ) Right, ...
Widex
FDA UDI
Widex A/S·05706069725643·Widex EVOKE E-CIC (Light beige S-110 ) Right, R...
MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·May 8, 2013
SHILEY LOW PRESSURE CUFFED
FDA Adverse Event
Injury
·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code JOH·May 19, 2011
CARPENTIER-EDWARDS PHYSIO MITRAL ANNULOPLASTY RING
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·August 6, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·August 21, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·August 5, 2021
'n'-Hole Post which is a component of the Revolution External Fixation System Catalog Numbers: 100801, 100802, 100803, 100804, 100805
FDA Recall
Open, Classified
·New Standard Device Inc·Product code KTT·July 23, 2019