22 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Disposable Surgical Mask
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113356·CLEAR CORNEA KNIFE 2.8MM (BX/5)
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113363·CLEAR CORNEA KNIFE 3.0MM (BX/5)
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113288·STAB KNIFE 22.5 DEGREE (BX/5)
NOBELACTIVE TIULTRA NP 3.5X13MM
FDA Adverse Event
Injury
·NOBEL BIOCARE AB·Product code DZE·May 31, 2021
NOBELACTIVE TIULTRA NP 3.5X13MM
FDA Adverse Event
Injury
·NOBEL BIOCARE AB·Product code DZE·May 31, 2021
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102457·MAXTM HXL Patella Component Sz 3 34mm 9.0mm Thick
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102464·MAXTM HXL Patella Component Sz 4 38mm 9.5mm Thick
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150793·Patella Instrument Case
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102440·MAXTM HXL Patella Component Sz 2 30mm 8.5mm Thick
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102471·MAXTM HXL Patella Component Sz 5 42mm 10.0mm Thick
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102433·MAXTM HXL Patella Component Sz 1 27mm 8.0mm Thick
TERABYTE 2000 HAIR REMOVER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
THERMAL CAUTERY UNIT, MODEL 150
FDA 510(k)
FDA Class 2
·Ophthalmic
EKOSONIC KIT 106CM 12CM TZ
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code KRA·November 16, 2023
BECKMAN-COULTER ANALYZER
FDA Adverse Event
Injury
·BECKMAN-COULTER·Product code GKZ·October 15, 2008
PARIETEX UGYTEX PP 15X10CM X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·June 21, 2013
SPACEMAKER PREPERITONEAL DIST BALLOON
FDA Adverse Event
Injury
·USSC PUERTO RICO·Product code GCJ·August 3, 2011
PULSE
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·August 22, 2024
VERSAPULSE POWERSUITE
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·August 19, 2024