18 results
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45ms
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Sources: EU EUDAMED, US FDA
SURGICAL INSTRUMENT MANUFACTURERS, LLC
FDA registration
SURGICAL INSTRUMENT MANUFACTURERS, LLC·1 product·🇺🇸 United States
Alamo T
FDA registration
ALLIANCE PARTNERS, LLC·1 product·🇺🇸 United States
ALAMO T
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699557·GENUMEDI PSS BLUE SIZE III
Bernafon
FDA UDI
Bernafon AG·05711584052488·JU7 ITCD, WL R BE JUNA 7
Extreme H2O 59% Xtra
FDA registration
Acucon·1 product·🇺🇸 United States
Sterigenics U.S., LLC
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Sterigenics US LLC
FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States
ADSON TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896076433·ADSON TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLAT...
Arthocare8208 (CR2) - Collagen Tendon Sheet-DDI
FDA registration
Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica
B. BRAUN SURGICAL, S.A.
FDA registration
B. BRAUN SURGICAL, S.A.·1 product·🇪🇸 Spain
Caya contoured diaphragm
FDA registration
KESSEL MEDINTIM GMBH·1 product·🇩🇪 Germany
CAYA Diaphragm
FDA registration
FEBANA GMBH·1 product·🇩🇪 Germany
59% EXTREME H2O (HIOXIFILCON A) SOFT CONTACT LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2076-XXYY, 2092-XXYY, 2105-XXYY
FDA 510(k)
FDA Class 2
·Cardiovascular
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Catheter, Percutaneous, Cutting/Scoring
FDA classification
FDA Class 2
·Catheter, Percutaneous, Cutting/Scoring
Lenses, Soft Contact, Daily Wear
FDA classification
FDA Class 2
·Lenses, Soft Contact, Daily Wear