Redapt Augments

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

Redapt Augments

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

Redapt Augments

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

REDAPT

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

REDAPT

FDA registration

PERRYMAN COMPANY·1 product·🇺🇸 United States

Redapt Augments

FDA registration

SMITH & NEPHEW, INC.·1 product·🇺🇸 United States

Smith & Nephew, Inc. REDAPT Augments

FDA 510(k)

FDA Class 2 ·Orthopedic

Solar 8000i

FDA registration

GE Medical Systems Information Technologies, Inc.·1 product·🇺🇸 United States

Hand Controller Pkg. Assy. (ED-800006)

FDA registration

Sterigenics US LLC·2 products·🇺🇸 United States

Solar 8000i

FDA registration

GE Medical Systems Information Technologies - Critikon de Mexico S. de R.L. de C.V.·1 product·🇲🇽 Mexico

Transport Pro

FDA registration

CANUTE INTERNATIONAL MEDICAL SERVICES (CANADA) INC·1 product·🇨🇦 Canada

Solar 8000i

FDA registration

GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·1 product·🇺🇸 United States

Ureteric catheters Floppy and Flush

FDA registration

Sterigenics SAS·1 product·🇫🇷 France

AESCULAP, INC.

FDA registration

AESCULAP, INC.·2 products·🇺🇸 United States

SURGIVISION INC. CLEARPOINT SYSTEM

FDA 510(k)

FDA Class 2 ·Neurology

SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE

FDA 510(k)

FDA Class 2 ·Cardiovascular

Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri

FDA classification

FDA Class 2 ·Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)