HARWOOD DESIGN, INC.

FDA registration

HARWOOD DESIGN, INC.·1 product·🇺🇸 United States

Sterigenics US, LLC

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Arch Medical Solutions - Elkhart

FDA registration

Arch Medical Solutions - Elkhart·1 product·🇺🇸 United States

FIRST ARTICLE INC

FDA registration

FIRST ARTICLE INC·1 product·🇺🇸 United States

EPTAM PLASTICS, LTD

FDA registration

EPTAM PLASTICS, LTD·1 product·🇺🇸 United States

BRANCH MEDICAL GROUP

FDA registration

BRANCH MEDICAL GROUP·1 product·🇺🇸 United States

ARCH Medical Solutions - Memphis

FDA registration

ARCH Medical Solutions - Memphis·1 product·🇺🇸 United States

FORTIFY Corpectomy Spacer

FDA registration

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

Pump MAX

FDA registration

Penumbra Inc.·1 product·🇺🇸 United States

FDR CROSS (DR-XD 3000)

FDA registration

FUJIFILM CORPORATION·2 products·🇯🇵 Japan

Reprocessed Mapping Catheter Sensor Enabled

FDA registration

INNOVATIVE HEALTH, LLC.·1 product·🇺🇸 United States

LevaLap Laparoscopic Access Device

FDA registration

J-PAC, LLC.·1 product·🇺🇸 United States

PENUMBRA PUMP MAX (110VAC), PENUMBRA PUMP MAX (230VAC), PENUMBAR PUMP MAX CANISTER/TUBING

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

FORTIFY(TM) AND FORTIFY(TM)-R CORPECTOMY SPACERS

FDA 510(k)

FDA Class 2 ·Orthopedic

Orthopedic Stereotaxic Instrument

FDA classification

FDA Class 2 ·Orthopedic Stereotaxic Instrument

Apparatus, Suction, Ward Use, Portable, Ac-Powered

FDA classification

FDA Class 2 ·Apparatus, Suction, Ward Use, Portable, Ac-Powered

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device