26 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NUVASIVE COROENT NO-PROFILE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
9300
FDA UDI
HANS RUDOLPH, INC.·00874750009039·9361 INSP OCCL SUB 2600 2WAY
G-Probe™ Single
FDA UDI
IRIDEX CORPORATION·00851089000234·
ORTHODONTIC CERAMIC BRACKET
FDA 510(k)
FDA Class 2
·Dental
VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HCV CONTROLS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
G PROBE
FDA Adverse Event
Injury
·IRIDEX CORPORATION·Product code GEX·July 8, 2008
G-PROBE SINGLE
FDA Adverse Event
Injury
·IRIDEX CORPORATION·Product code GEX·April 1, 2016
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·March 10, 2022
COULTER® LH 750 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 14, 2013
GRANUFLO
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 10, 2014
BRAVO
FDA Adverse Event
Malfunction
·GIVEN IMAGING LTD.·Product code FFT·May 26, 2011
VANGUARD CR ILOK FEM-RT 67.5
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·January 30, 2019
UNK - IMPLANT
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·February 2, 2026
UNK - IMPLANT
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·January 30, 2026
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·September 4, 2009
IRIDEX G-PROBE
FDA Adverse Event
Malfunction
·IRIDEX CORPORATION·Product code GEX·July 3, 2015
UNK - IMPLANT
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·February 2, 2026
UNK - IMPLANT
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·February 2, 2026
UNK - IMPLANT
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·February 2, 2026
UNK - IMPLANT
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·February 2, 2026