3,294 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT II (POLYMACON)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT II (POLYMACON)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT II (POLYMACON)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT II (POLYMACON)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT II (POLYMACON)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT II (POLYMACON)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT(TM) (DELTAFILCON A)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT(TM) (DELTAFILCON A)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SOFTACT(TM) (DELTAFILCON A)
ProVate Vaginal Support
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
DISCON DAILY (ETAFILCON A) ONE-DAY SOFT (HYDROPHILIC) CONTACT LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFICATION TO OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Cardiovascular
Pegavision (Hioxifilcon A) One-Day Soft (Hydrophilic) Contact Lenses (59% Water)
FDA 510(k)
FDA Class 2
·Ophthalmic
Anterior Spine Truss System Stand Alone (ASTS-SA) Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
SENSOMAT MUSCLE/TISSUE PH
FDA 510(k)
FDA Class 2
·Anesthesiology
CDI(R) 2000 BLOOD GAS MONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
PARATREND 7 MULTIPARAMETER SENIOR AND SATELLITE MONITOR SYSTEM WITH PARATREND 7 PLUS MULTIPARAMETER SENSOR
FDA 510(k)
FDA Class 2
·Anesthesiology
MODEL PB3300 INTRA-ARTER BLOOD GAS MONIT SYS, MODI
FDA 510(k)
FDA Class 2
·Anesthesiology