948 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·FLUOREX (TM) 600 (FLURSILFOCON A)
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·RIGID GAS PERMEABLE CONTACT LENSES
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·NOVALENS (ROSILFOCON A)
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·FLUOROPERM 60 (PAFLUFOCON B) CONTACT LENS
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·FLUOREX (TM) 600 (FLURSILFOCON A)
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·OCUSIL(TM) CONTACT LENS
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·BOSTON EQUALENS(R) AND BOSTON RXD(R)
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·OCUSIL(TM) CONTACT LENS
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·RIGID GAS PERMEABLE CONTACT LENSES
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·PARAPERM E.W. (PASIFOCON C) RGP CONTACT LENS
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·OPTACRYL K
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·THE BOSTON EQUALENS (FLUROFOCON A) CONTACT LENS
Sterilizer, Soft-Lens, Thermal, Ac-Powered
FDA Pre-Market Approval
FDA Class 2
·HYDROCURVE PATIENT DISINFECTION UNIT
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·O-PERM F60 RGP CONTACT LENS
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·OPTACRYL 60 - CLEAR
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
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE
Ventilator, Non-Continuous (Respirator)
FDA classification
FDA Class 2
·Ventilator, Non-Continuous (Respirator)
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, BP/LORDOTIC DEVICE