948 results · 21ms · Sources: EU EUDAMED, US FDA

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