8ch Knee SPEEDER

FDA registration

QUALITY ELECTRODYNAMICS·1 product·🇺🇸 United States

8 CH Knee SPEEDER

FDA 510(k)

FDA Class 2 ·Radiology

Genesis

FDA UDI

KEYSTONE DENTAL, INC.·D768K156950·Ratchet

Modpod

FDA registration

HOLLYWOG, LLC·1 product·🇺🇸 United States

CryotopCL

FDA registration

KITAZATO CORPORATION·1 product·🇯🇵 Japan

CryotopCL

FDA registration

RADIA INDUSTRY CO., LTD.·1 product·🇯🇵 Japan

Ophthalmic Speculum

FDA UDI

KATENA PRODUCTS, INC.·00841668100622·KATENA DOUBLE-X SPECULUM V-WIRE

USHIO GERMANY GmbH

FDA registration

USHIO GERMANY GmbH·1 product·🇩🇪 Germany

Ushio Poland SP. z o.o

FDA registration

Ushio Poland SP. z o.o·1 product·🇵🇱 Poland

ORTA MEDICAL LTD

FDA registration

ORTA MEDICAL LTD·1 product·🇮🇱 Israel

CRYOTOP

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

SURETEK MEDICAL REPROCESSED ARTHROSCOPIC BLADES AND BURS

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Coil, Magnetic Resonance, Specialty

FDA classification

FDA Class 2 ·Coil, Magnetic Resonance, Specialty

Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

FDA classification

FDA Class 2 ·Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Labware, Assisted Reproduction

FDA classification

FDA Class 2 ·Labware, Assisted Reproduction