AccelFix Lumbar Expandable Cage System

FDA registration

L&K BIOMED CO.,LTD.·1 product·🇰🇷 South Korea

AccelFix Lumbar Interbody Fusion Cage System

FDA 510(k)

FDA Class 2 ·Orthopedic

Ophthalmic Retractor

FDA UDI

KATENA PRODUCTS, INC.·00841668101070·WALTON CONJUNCTIVA RETRACTOR

Hayden Medical

FDA UDI

Hayden Medical, Inc.·00840319741832·Spratt (Brun) Bone Curette 6-1/2" (16.3cm), siz...

Equinoxe Reverse Shoulder Superior Augment Glenoid Plate

FDA registration

Exactech Sarasota·3 products·🇺🇸 United States

Equinoxe Reverse Shoulder Superior Augment Glenoid Plate

FDA registration

EXACTECH, INC.·3 products·🇺🇸 United States

ONETOUCH VERIO SYNC BLOOD GLUCOSE MONITORING SYSTEM

FDA registration

Flextronics Industrial (Shenzhen) Co., Ltd.·2 products·🇨🇳 China

Isomedix Operations, Inc.

FDA registration

Isomedix Operations, Inc.·3 products·🇺🇸 United States

OneTouch Verio Sync Blood Glucose Monitorning System

FDA registration

LIFESCAN EUROPE GMBH·2 products·🇨🇭 Switzerland

OneTouch Verio Test Strips

FDA registration

LIFESCAN SCOTLAND LTD·2 products·🇬🇧 United Kingdom

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·3 products·🇺🇸 United States

syngo.Interventional

FDA UDI

Siemens Healthcare GmbH·04056869248653·syngo.Interventional VB40; Medical Device syngo...

Medicom Pediatric Mask

FDA registration

AMD Medicom Inc.·1 product·🇨🇦 Canada

MAINLINE MEDICAL DENTAL SUPPLY

FDA registration

MAINLINE MEDICAL DENTAL SUPPLY·1 product·🇨🇦 Canada

EQUINOXE REVERSE SHOULDER COMPRESSION SCREW / 38MM AND 42MM GLENOSPHERE / SUPERIOR AUGMENT GLENOID PLATE, 10 DEGREES...

FDA 510(k)

FDA Class 2 ·Orthopedic

PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES

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

Shoulder Prosthesis, Reverse Configuration

FDA classification

FDA Class 2 ·Shoulder Prosthesis, Reverse Configuration

Appliance, Fixation, Spinal Intervertebral Body

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body