18 results · 45ms · 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