Synergeyes, Inc. is one of 13008 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synergeyes, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SynergEyes A&M (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes KC (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes PS (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes SiH (petrafocon A hem-larafilcon A) Hybrid Daily Wear Contact Lens, SynergEyes UltraHealth for Keratoconus (petrafocon A hem-larafilcon A) Hybrid Daily Wear Co, SynergEyes SiH with Hydra-PEG(petrafocon A hem-larafilcon A) Hybrid Daily Wear Lens, UltraHealth Hybrid Contact Lens for Keratoconus, UltraHealth Flat Cornea Hybrid Contact Lens
Synergeyes, Inc. has 9 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 9 cleared submissions from 2006 to 2016. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Synergeyes, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by R.E. Lippman Regulatory Pathways and Eyereg Consulting, Inc..