ENDO Dual

FDA registration

SATELEC-ACTEON GROUP·1 product·🇫🇷 France

I-ENDO DUAL

FDA 510(k)

FDA Class 1 ·Dental

Controller, Foot, Handpiece And Cord

FDA classification

FDA Class 1 ·Controller, Foot, Handpiece And Cord

Bone cutters

FDA UDI

DFS - DIAMON GmbH·04057176148018·Bone Cutter type 162 FG

n/a

FDA UDI

Ortho Development Corporation·00822409076154·Femoral Broach/Trial 1623

St. Jude Medical, Cardiology Division, Inc.

FDA registration

St. Jude Medical, Cardiology Division, Inc.·1 product·🇺🇸 United States

ABBOTT LABORATORIES

FDA registration

CENTERPIECE S. DE R.L DE C.V (sterilization site)·1 product·🇲🇽 Mexico

Exeter Hip System

FDA registration

STRYKER IRELAND OSTEONICS·1 product·🇮🇪 Ireland

Lisi34951 (ED) - Exeter Hip System

FDA registration

Synergy Health Westport Ltd·1 product·🇮🇪 Ireland

LISI MEDICAL ORTHOPAEDICS

FDA registration

LISI MEDICAL ORTHOPAEDICS·1 product·🇫🇷 France

IRVINE BIOMEDICAL. INC.

FDA registration

IRVINE BIOMEDICAL. INC.·1 product·🇺🇸 United States

Lisi34951 (ED) - Exeter Hip System

FDA registration

Synergy Health Ede BV·1 product·🇳🇱 Netherlands

St. Jude Medical

FDA registration

St. Jude Medical·1 product·🇺🇸 United States

MicroSelectron Digital

FDA UDI

Nucletron B.V.·08717213026285·microSelectron Transfer Tube for 5F Flexibles (27)

Panoramic P200T (Daytona)

FDA registration

Optos Inc.·1 product·🇺🇸 United States

Endoskeleton TAS IBD

FDA registration

PERRYMAN COMPANY·1 product·🇺🇸 United States

UNIMAX MEDICAL SYSTEMS INC.

FDA registration

UNIMAX MEDICAL SYSTEMS INC.·1 product·🇹🇼 Taiwan

EXETER HIP SYSTEM WITH V40 TAPER

FDA 510(k)

FDA Class 2 ·Orthopedic

INQUIRY AFOCUSII DIAGNOSTIC CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Electrode Recording, Or Probe, Electrode Recording

FDA classification

FDA Class 2 ·Catheter, Electrode Recording, Or Probe, Electrode Recording