84 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KOWA VX-20
FDA 510(k)
FDA Class 2
·Ophthalmic
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950017447·RETRACTOR SURGICAL CURVED DOWN 7X25MM 8-1/2" 21CM
NA
FDA UDI
MAKO SURGICAL CORP.·00848486002954·FEMORAL ARRAY
AOS TIBIAL NAIL 12mm x 33.0cm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016314·
Centric Duo Lateral Retractor
FDA UDI
Life Spine, Inc.·00190837034764·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024493476·
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776180089·Tissue Forceps teeth
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00846795000548·
Experience
FDA UDI
Gc Orthodontics America Inc.·E53511233000301·EXC XT 022/LL3 -3T 7A 2M
Experience
FDA UDI
Gc Orthodontics America Inc.·D78811233000101·EXC ROTH 022/LL3 -11T 7A 2M
Experience
FDA UDI
Gc Orthodontics America Inc.·D78811233000301·EXC XT 022/LL3 -3T 7A 2M
Experience
FDA UDI
Gc Orthodontics America Inc.·E53511233000101·EXC ROTH 022/LL3 -11T 7A 2M
AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
SIMPLICITY EURO QD INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100798·L CR Cemented Femoral Component Sz 3N
BE-PLS 2050
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 26, 2014
BE-PLS 2050 PERMENANT LIFE SUPPORT
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code KFM·March 6, 2014
BE-PLS 2050 PERMENANT LIFE SUPPORT
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 27, 2014
HLS SET
FDA Adverse Event
Death
·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·August 18, 2025
TUBING SET
FDA Adverse Event
Death
·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·April 28, 2025