46 results
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49ms
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Sources: EU EUDAMED, US FDA
CS Tianjin Lancet Multiple Use
FDA registration
I-SENS USA, INC.·2 products·🇺🇸 United States
Prodigy Adjustable Depth Lancing Device
FDA registration
PRODIGY DIABETES CARE, LLC·2 products·🇺🇸 United States
TENOVI CO
FDA registration
TENOVI CO·2 products·🇺🇸 United States
Twist-off Lancet lancet
FDA registration
TIANJIN HUADA HONGYI BIOTECHNOLOGY CO., LTD.·2 products·🇨🇳 China
Lancet
FDA registration
ARKRAY Industry West Inc.·1 product·🇵🇭 Philippines
Lancet (I, II, III, V, VI); Lancing device (HH-X-T, HH-XIII-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Multiple Use Blood Lancet For Single Patient Use Only
FDA classification
FDA Class 2
·Multiple Use Blood Lancet For Single Patient Use Only
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113523·SLIT BLADE 3.0MM STR (BX/5)
IDS-iSYS Ostase® BAP
FDA registration
EUROIMMUN US INC.·1 product·🇺🇸 United States
IDS-iSYS Ostase® BAP
FDA registration
IMMUNODIAGNOSTIC SYSTEMS LTD.·1 product·🇬🇧 United Kingdom
Biotornix Healthcare Quincke Spinal Needle
FDA registration
BIOTRONIX HEALTHCARE INDUSTRIES INC.·1 product·🇺🇸 United States
LUMBAR PUNCTURE NEEDLE
FDA registration
CROSSMED MEDICAL DEVICE CO., LTD·1 product·🇻🇬 Virgin Islands, British
Lumbar Puncture Needles
FDA registration
NEOCHILD, LLC·1 product·🇺🇸 United States
ANESTHESIA CONDUCTION NEEDLES
FDA registration
SHANGHAI SA MEDICAL & PLASTIC INSTRUMENTS CO., LTD.·1 product·🇨🇳 China
NEUWAVE Microwave Ablation
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
EQ-M
FDA registration
META SYSTEMS CO., LTD also doing business as S-Denti Co.,Ltd·2 products·🇰🇷 South Korea
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996120708·LATERAL,SPACER 22,45X7.5,0 DEG
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996120722·LATERAL,SPACER 22,55X7.5,0 DEG
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996120715·LATERAL,SPACER 22,50X7.5,0 DEG
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996120746·LATERAL,SPACER 22,65X7.5,0 DEG