VYRSA V1 Sacroiliac Transfixing and Fusion System

FDA registration

GLOBUS MEDICAL, INC.·1 product·🇺🇸 United States

Camber Sacroiliac (SI) Fixation System

FDA 510(k)

FDA Class 2 ·Orthopedic

Sacroiliac Joint Fixation

FDA classification

FDA Class 2 ·Sacroiliac Joint Fixation

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

Scorpio Knee System

FDA registration

HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

ALMARK TOOL & MANUFACTURING COMPANY, INC.

FDA registration

ALMARK TOOL & MANUFACTURING COMPANY, INC.·1 product·🇺🇸 United States

Aspire Cristalle FDR MS-3500

FDA registration

FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·1 product·🇯🇵 Japan

Aspire Cristalle FDR MS-3500

FDA registration

FUJIFILM CORPORATION·1 product·🇯🇵 Japan

Scorpio Knee System

FDA registration

STRYKER IRELAND OSTEONICS·1 product·🇮🇪 Ireland

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

KEN-MAR MACHINE MFG CORP

FDA registration

KEN-MAR MACHINE MFG CORP·1 product·🇺🇸 United States

DaylightRx

FDA registration

BIG HEALTH INC·1 product·🇺🇸 United States

CEREGLIDE 92 Catheter System

FDA registration

Cerenovus, Inc.·1 product·🇲🇽 Mexico

Alcon Research, LLC

FDA registration

Alcon Research, LLC·1 product·🇺🇸 United States

SCORPIO TOTAL KNEE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

ASPIRE CRISTALLE

FDA 510(k)

FDA Class 2 ·Radiology

Full Field Digital, System, X-Ray, Mammographic

FDA classification

FDA Class 2 ·Full Field Digital, System, X-Ray, Mammographic

Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer