10,000 results
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89ms
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Sources: EU EUDAMED, US FDA
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258658179·FIX SUPER MAX ZIP ANCHOR SELF PUNCHING Ø2,6mm F...
Timm Medical
FDA UDI
POS-T-VAC INC·00857312008053·
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258658216·FIX SUPER MAX ZIP ANCHOR SELF PUNCHING Ø2,6mm 2...
NuVasive Maximum Viscosity Spinal Cement System
FDA UDI
TEKNIMED·03760177047396·
NL400
FDA UDI
NAKANISHI INC.·04560264573260·
CLEO ADVANTAGE
FDA UDI
NARVA Lichtquellen GmbH + Co KG.·04014501004043·
Perfect Bronze
FDA UDI
NARVA Lichtquellen GmbH + Co KG.·04014501003787·
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258659008·FIX SUPER MAX ZIP ANCHOR Ø2,6 FIXED TAPE 1,3mm ...
FRESH Bold Impression Material
FDA UDI
EXACTA DENTAL PRODUCTS INC·00815619020628·FRESH Bold Impression Material Blu Max Bite Reg...
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258658162·FIX SUPER MAX ZIP ANCHOR SELF PUNCHING Ø2,6mm F...
DynaFORCE
FDA UDI
CROSSROADS EXTREMITY SYSTEMS·00815432026104·MotoCLIP/HiMAX Implant System is a Nitinol Supe...
Gafchromic™
FDA UDI
ASHLAND SPECIALTY INGREDIENTS G.P.·00850000065567·
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258658995·FIX SUPER MAX ZIP ANCHOR Ø2,6 FIXED TAPE 1,3mm ...
Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258658209·FIX SUPER MAX ZIP ANCHOR SELF PUNCHING Ø2,6mm 2...
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX THREADED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·VISTA LORDOTIC INTERBODY FUSION CAGE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE