CLEARLAKE-TECH INC

FDA registration

CLEARLAKE-TECH INC·1 product·🇺🇸 United States

Iomed

FDA registration

DJO, LLC·1 product·🇺🇸 United States

RH-806/GS MODEL TRANSQ(R)2

FDA 510(k)

FDA Class 2 ·Physical Medicine

Device, Iontophoresis, Other Uses

FDA classification

FDA Class 2 ·Device, Iontophoresis, Other Uses

MAGNETIC TOOL PAD

FDA UDI

ALIMED, INC.·00733657218107·

STERIS SPA

FDA registration

STERIS SPA·2 products·🇮🇹 Italy

Vertebrex Kyphoplasty Catheter (Flex)/Kit; Vertebrex Kyphoplasty Catheter (Micro)/Kit; Vertebrex Kyphoplasty Catheter (Mini)/Kit;

FDA registration

ZAVATION·2 products·🇺🇸 United States

INTERNATIONAL STERILIZATION LABORATORY, LLC

FDA registration

INTERNATIONAL STERILIZATION LABORATORY, LLC·2 products·🇺🇸 United States

LRX

FDA registration

GLOBAL PACKAGING SYSTEMS INC·1 product·🇺🇸 United States

KYPHOPLASTY BALLOON CATHETER

FDA registration

BIOPSYBELL S.R.L.·2 products·🇮🇹 Italy

Case Contact Lens

FDA registration

BRISAR INDUSTRIES INC·1 product·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

INTER V KYPHOPLASTY CATHETER (BALLOON LENGTH: 0 MM), INTERV KYPHOPLASTY CATHETER (BALLOON LENGHT: 15 MM), INTERV KYPHOPL

FDA 510(k)

FDA Class 2 ·Orthopedic

GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

Cement, Bone, Vertebroplasty

FDA classification

FDA Class 2 ·Cement, Bone, Vertebroplasty

System, Imaging, Pulsed Doppler, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Doppler, Ultrasonic