OSPREY Midline Closed IV Catheter System (OspreyEDC-F20)

FDA registration

SKYDANCE VASCULAR, INC.·1 product·🇺🇸 United States

OSPREY Midline Closed IV Catheter System (OspreyEDC-F20)

FDA 510(k)

FDA Class 2 ·General Hospital

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776183394·Hoke Osteotome cvd

Integra® Jarit®

FDA UDI

INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780455905·Integra® Jarit® Hoke Osteotome, Curved

Wax, Bone

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

Wax, Bone - DeRoyal

FDA registration

DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

Disposable Endoscope Injection Needle

FDA registration

YANGZHOU FARTLEY MEDICAL INSTRUMENT TECHNOLOGY CO., LTD·1 product·🇨🇳 China

Wax, Bone - DeRoyal

FDA registration

DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

DIAGNOSTICO MEDICO SAC

FDA registration

DIAGNOSTICO MEDICO SAC·1 product·🇵🇪 Peru

Sharpoint

FDA registration

Surgical Specialties Mexico S DE RL DE CV·1 product·🇲🇽 Mexico

Wax, Bone - DeRoyal

FDA registration

DeRoyal Industries, Inc.·1 product·🇺🇸 United States

Wax, Bone - DeRoyal

FDA registration

DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

JD28-3095

FDA registration

L&K BIOMED CO.,LTD.·1 product·🇰🇷 South Korea

SHARPOINT LUKENS BONE WAX

FDA 510(k)

FDA Unclassified ·Unknown

Chocolate PTCA Balloon Catheter

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

FDA classification

FDA Class 2 ·Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Wax, Bone

FDA classification

FDA Unclassified ·Wax, Bone

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA classification

FDA Class 2 ·Catheters, Transluminal Coronary Angioplasty, Percutaneous