InterX Self-Adhesive Dual Electrode - Non-Sterile

FDA registration

SVTRONICS, INC.·1 product·🇺🇸 United States

InterX Self-Adhesive Dual Electrode - Non-Sterile

FDA registration

InterX Technologies·1 product·🇺🇸 United States

INTERX STERILE SELF-ADHESIVE DUAL ELECTRODE (ISSDE)

FDA 510(k)

FDA Class 2 ·Neurology

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04049772814749·GENUMEDI EXTRA WIDE SAND SIZE VI

Parietex™ Optimized Composite Mesh

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

Parietex

FDA registration

CEVA LOGISTICS·1 product·🇳🇱 Netherlands

PK Superpulse System Generator Model 744000

FDA registration

Arvato SE·2 products·🇩🇪 Germany

PK Superpulse System Generator Model 744000

FDA registration

GYRUS MEDICAL LTD.·2 products·🇬🇧 United Kingdom

Synergy Health Sterilisation UK Ltd

FDA registration

Synergy Health Sterilisation UK Ltd·2 products·🇬🇧 United Kingdom

Raw Surgical Corporation

FDA UDI

RAW SURGICAL CORPORATION·G508RSC11308160·DEBAKEY TISSUE FORCEPS, Jaws 2mm wide, Overall ...

K2M General Instruments

FDA UDI

K2M, INC.·10888857562486·Lordotic Trial Size 22x50x14 mm, 8°

Strattice Reconstructive Tissue Matrix (RTM) Laparoscopic

FDA registration

LIFECELL CORP·2 products·🇺🇸 United States

Synergy Health AST, LLC

FDA registration

Synergy Health AST, LLC·2 products·🇺🇸 United States

Dilator, Vessel, Surgical - DeRoyal

FDA registration

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

FLEX Monoclonal Mouse Anti-Human Progesterone Receptor, Clone PgR 636, Ready-to-Use (Link)

FDA registration

Agilent Technologies, Inc.·1 product·🇺🇸 United States

Dilator, Vessel, Surgical - DeRoyal

FDA registration

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

PK SUPERPULSE SYSEM GENERATOR MODEL 744000

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

MSD CABLE REDUCTION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Electrode, Cutaneous

FDA classification

FDA Class 2 ·Electrode, Cutaneous

Appliance, Fixation, Spinal Interlaminal

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Interlaminal