124 results
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35ms
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Sources: EU EUDAMED, US FDA
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTICS (DELTAFILCON A) LENS
ReLine
FDA UDI
Nuvasive, Inc.·00887517010520·RELINE-C Handle, Torque 26in-lbs
Trimline
FDA UDI
ORMCO CORPORATION·00889989050875·UPPER RIGHT FIRST MOLAR TRIMLINE BAND SIZE 15
SERUM, CREATININE PHOSPHOKINASE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Continuum® Trilogy® Allofit®
FDA UDI
Zimmer, Inc.·00889024152380·
Continuum® Trilogy® Allofit®
FDA UDI
Zimmer, Inc.·00889024152397·
Continuum® Trilogy® Allofit®
FDA UDI
Zimmer, Inc.·00889024152403·
Continuum® Trilogy® Allofit®
FDA UDI
Zimmer, Inc.·00889024152427·
Continuum® Trilogy® Allofit®
FDA UDI
Zimmer, Inc.·00889024152410·
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·TREO® Abdominal Stent-Graft System
System, Test, Her-2/Neu, Ihc
FDA Pre-Market Approval
FDA Class 3
·BOND ORACLE HER2 IHC SYSTEM
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Malfunction
·BOLTON MEDICAL, INC.·Product code MIH·July 12, 2022
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·February 16, 2021
HILL ROM CENTRELLA
FDA Adverse Event
Injury
·HILL-ROM, INC.·Product code FNL·January 31, 2025
HILL ROM CENTRELLA
FDA Adverse Event
Injury
·HILL-ROM, INC.·Product code FNL·January 31, 2025
HILL ROM CENTRELLA
FDA Adverse Event
Injury
·HILL-ROM, INC.·Product code FNL·January 31, 2025
HILL ROM CENTRELLA
FDA Adverse Event
Injury
·HILL-ROM, INC.·Product code FNL·January 31, 2025
HILL ROM CENTRELLA
FDA Adverse Event
Injury
·HILL-ROM, INC.·Product code FNL·January 31, 2025
HILL ROM CENTRELLA
FDA Adverse Event
Injury
·HILL-ROM, INC.·Product code FNL·January 31, 2025
HILL ROM CENTRELLA
FDA Adverse Event
Injury
·HILL-ROM, INC.·Product code FNL·January 31, 2025