SeaSpine Spacer System NM

FDA registration

SEASPINE ORTHOPEDICS CORPORATION·2 products·🇺🇸 United States

Millstone Medical Outsourcing LLC

FDA registration

Millstone Medical Outsourcing LLC·2 products·🇺🇸 United States

SEASPINE SPACER SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04049772814695·GENUMEDI SILVER SIZE VI

Mini Master Series

FDA UDI

AMERICAN ORTHODONTICS CORPORATION·00190746108501·DB BRACKET MINI MS MAX LEFT CUSPID 022 TQ=+8 A=...

ALL SILICONE FOLEY BALLOON CATHETER

FDA UDI

Sewoon Medical Co., Ltd.·08806369402620·2way/Translucent 30cc 26fr

KEN-MAR MACHINE MFG CORP

FDA registration

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

Trident Acetabular System

FDA registration

HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

ISOMEDIX OPERATIONS INC.

FDA registration

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

ISOMEDIX OPERATIONS INC.

FDA registration

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

Affinity Pixie¿ Arterial Filter with Balance¿ Biosurface

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Affinity Pixie¿ Arterial Filter with Balance¿ Biosurface

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

MARSON MEDICAL, INC.

FDA registration

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

CROC

FDA registration

SAFEGUARD US OPERATING, LLC·1 product·🇺🇸 United States

"QUADROX-iR Adult / Small Adult, with and without integrated Arterial Filter, with BIOLINE or SOFTLINE Coating;

FDA registration

Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

ES-BC

FDA registration

LD TECHNOLOGY·1 product·🇺🇸 United States

"QUADROX-iR Adult / Small Adult, with and without integrated Arterial Filter, with BIOLINE or SOFTLINE Coating;

FDA registration

Sterigenics Germany GmbH·1 product·🇩🇪 Germany

CAPIOX ARTERIAL FILTER

FDA 510(k)

FDA Class 2 ·Cardiovascular

TRIDENT ALL POLY CUP

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar