17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NightOwl
FDA 510(k)
FDA Class 2
·Anesthesiology
LEONE SPA
FDA UDI
LEONE SPA·08033707022220·CALIBRA BANDS 2ND MOLAR n.SUR 28
Surgical Connector Kit
FDA UDI
Synapse Biomedical, Inc.·00852184003410·
AQUAMAX (ETAFILCON A) DISPOSABLE SOFT CONTACT LENSES
FDA 510(k)
FDA Class 2
·Ophthalmic
6F MACH1/34356-XXX; 5F MACH1/35845-XXX; 7F MACH1/34357-XXX; 8F MACH1/34358-XXX
FDA 510(k)
FDA Class 2
·Cardiovascular
RELAY THORACIC STENT-GRAFT WITH PLUS DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·November 7, 2019
Widex
FDA UDI
Widex A/S·05706069797107·Widex D-CIC (Clay brown ) Dream 220, Left, RC coil
Widex
FDA UDI
Widex A/S·05706069887082·WIDEX MOMENT M-IP (Clay brown ) 220, Right
Widex
FDA UDI
Widex A/S·05706069796681·Widex EVOKE E-CIC (Clay brown ) 220, Left, RC coil
Widex
FDA UDI
Widex A/S·05706069819816·Widex UNIQUE U-IP (Clay brown ) 220, Right
Widex
FDA UDI
Widex A/S·05706069796919·Widex EVOKE E-IP (Clay brown ) 220, Right
Widex
FDA UDI
Widex A/S·05706069888959·WIDEX MOMENT M-CIC (Clay brown ) 220, Left
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 3, 2014
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·August 12, 2011
QUADRA ASSURA CRT-D, DF4 CONNECTOR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·July 11, 2013
DAVINCI 5
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·March 25, 2026
CLS SPOTORNO, STEM, 135, UNCEMENTED, 10.0, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·March 20, 2018