1,076 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·Cordis S.M.A.R.T. CONTROL and S.M.A.R.T. Vascular Stent System
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (SENOFILCON A) BRAND CONTACT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (ETAFILCON A) BRAND CONTACT LENSES
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SOFTEC HD INTRAOCULAR LENS
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·Cordis® S.M.A.R.T.® CONTROL® and S.M.A.R.T.® Vascular Stent System
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ClearView 3
Joint, Temporomandibular, Implant
FDA Pre-Market Approval
FDA Class 3
·TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (senofilcon A) Brand Contact Lenses
Stent, Renal
FDA Pre-Market Approval
FDA Class 3
·PALMAZ Balloon Expandable Stent
Stent, Renal
FDA Pre-Market Approval
FDA Class 3
·CORDIS PALMAZ BALLOON EXPANDABLE STENTS
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·Cordis® S.M.A.R.T.® CONTROL® Nitinol Stent Systems, Cordis® S.M.A.R.T.® and S.M.A.R.T.® CONTROL® Vascular Stent Systems,
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (SENOFILCON A) BRAND CONTACT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (senofilcon A) Brand Contact Lenses
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·CORDIS EXOSEAL VASCULAR CLOSURE DEVICE
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODEL P11 MODIFIED J LOOP POSTERIOR CHAMBER IOL
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·CORDIS PRECISE NITINOL STENT SYSTEMS
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (SENOFILCON A) CONTACT LENS, CLEAR AND VISIBILITY TINTED WITH UV BLOCKER
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·Senofilcon A Reactive Monomer Mix (RMM) Batches
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODEL P13 MODEIFIED C LOOP POSTERIOR CHAMBER
Test, Urea Adult And Pediatric (Breath),
FDA Pre-Market Approval
FDA Class 3
·PyloPlus® UBT System