118 results · 20ms · Sources: EU EUDAMED, US FDA

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Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·BRANTIGEN I/F CAGE(R) USED WITH VSP(R) SPINE PLATES AND PEDICLE SCREWS

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE WITH VSP SPINAL SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE(R) SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE WITH VSP SPINE SYSTEM

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·SABER LUMBAR I/F CAGE, JAGUAR LUMBAR I/F CAGE

Spinal Pedicle Screw, Fixation, Appliance System

FDA Pre-Market Approval
FDA Class 3 ·LUMBAR I/F CAGE SYSTEM

Acrometrix MSSA Positive Control

FDA UDI
Microgenics Corporation·00884883006379·

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600251·Mand. 2. Molar band W-Fit left 25

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600250501·Mand. 2. Molar band W-Fit left 25

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600250101·Mand. 2. Molar band W-Fit left 25

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89600250051·Mand. 2. Molar band W-Fit left 25

PROTEK LOW PROFILE ACETABULAR CUP

FDA 510(k)
FDA Class 2 ·Orthopedic

Stent, Superficial Femoral Artery

FDA Pre-Market Approval
FDA Class 3 ·ASTRON PULSAR STENT SYSTEM, PULSAR-18 STENT SYSTEM

Heart-Valve, Non-Allograft Tissue

FDA Pre-Market Approval
FDA Class 3 ·ATS 3F AORTIC BIOPROSTHESIS