DuraFuse

FDA registration

NEURAMEDICA INC.·1 product·🇺🇸 United States

DuraFuse

FDA registration

Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States

DuraFuse

FDA registration

PEPIN MFG., INC.·1 product·🇺🇸 United States

DuraFuse Clip and Applier System

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04051526799448·MANUMED ACTIVE WRIST RIGHT SAND M

Clip, Implantable

FDA classification

FDA Class 2 ·Clip, Implantable

EYE-SYNC

FDA UDI

SYNC-THINK, INC.·00868096000300·

Arrow VPS G4

FDA registration

Arrow International, LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

SentrySuite Product Line 2.5

FDA registration

Jaeger Medical America Inc.·3 products·🇺🇸 United States

Arrow VPS G4

FDA registration

Arrow International LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

Arrow VPS G4 System

FDA registration

Teleflex Medical de Tecate, S. de R.L de C.V.·1 product·🇲🇽 Mexico

SentrySuite Product Line 2.5

FDA registration

Jaeger Medical GmbH·3 products·🇩🇪 Germany

Arrow VPS G4 System

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

Arrow VPS G4

FDA registration

Teleflex LLC (NADC 2)·1 product·🇺🇸 United States

SiJoin T3

FDA registration

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

CHOICARE Sterile Single-use LDV Syringe

FDA registration

JEIL TECH CO.,LTD·2 products·🇰🇷 South Korea

SENTRYSUITE PRODUCT LINE

FDA 510(k)

FDA Class 2 ·Anesthesiology

MODIFICATION TO:APEX MEDICAL IF-4100

FDA 510(k)

FDA Class 2 ·Neurology

Calculator, Predicted Values, Pulmonary Function

FDA classification

FDA Class 2 ·Calculator, Predicted Values, Pulmonary Function

Electrode, Cutaneous

FDA classification

FDA Class 2 ·Electrode, Cutaneous