Reprocessed External Fixation Device

FDA registration

Stryker Sustainability Solutions·3 products·🇺🇸 United States

component, traction, invasive Reprocessed External Fixation Devices

FDA registration

Sterigenics US LLC·3 products·🇺🇸 United States

Reprocessed External Fixation Device

FDA registration

Stryker Sustainability Solutions Phoenix·3 products·🇺🇸 United States

REPROCESSED EXTERNAL FIXATION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

Appliance, Fixation, Nail/Blade/Plate Combination, Single Component

FDA classification

FDA Class 2 ·Appliance, Fixation, Nail/Blade/Plate Combination, Single Component

AML HIP - RAW MATERIAL CHANGE FROM CAST TO FORGED (FROM ORIG. K012364)

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

SOLUTION SYSTEM HIP PROSTHESIS (DESIGN CHANGES TO VISION K953703 & AML K012364) SPECIAL 510(K)

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

Zirlux

FDA UDI

HENRY SCHEIN, INC.·00304040133316·Zirlux TR B3 98x22mm

MEDRAD® Veris™ 8600 Vital Signs Monitor

FDA UDI

BAYER MEDICAL CARE INC.·00616258009612·"PROBE, PULSE OX, GRIP, LARGE, 2M, VERIS (ASSY,...

Contour Meniscus Arrow

FDA registration

CONMED CORPORATION·1 product·🇺🇸 United States

Contour Meniscus Arrow

FDA registration

Linvatec Corporation d/b/a ConMed Linvatec·1 product·🇺🇸 United States

Contour Meniscus Arrow

FDA registration

Sterigenics U.S. LLC·1 product·🇺🇸 United States

Contour Meniscus arrow

FDA registration

BBF STERILISATIONSSERVICE GMBH·1 product·🇩🇪 Germany

Coblation

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

Contour Meniscus Arrow

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Coblation

FDA registration

ArthroCare Corporation·1 product·🇺🇸 United States

Coblation

FDA registration

Arthrocare Corporation·1 product·🇨🇷 Costa Rica

UNBRANDED

FDA UDI

FGX INTERNATIONAL INC.·00193033430347·

ARTHROCARE CONTROLLER, MODEL H2000; ARTHROCARE CABLE, MODEL H0970-02; FOOTSWITCH, MODEL H2000-04; POWERCORD, MODEL H2000

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

HEARTSTREAM XL DEFIBIBRILLATOR/MONITOR, MODEL M4735A, HEARTSTREAM XLT DEFIBRILLATOR/MONITOR.MODEL M2500B

FDA 510(k)

FDA Class 3 ·Cardiovascular