Synergeyes, Inc. is one of 4743 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synergeyes, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Synergeyes, Inc.
9 devices
Cleared
Nov 15, 2016
SynergEyes A&M (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact...
Ophthalmic
327d
Cleared
Aug 01, 2016
SynergEyes SiH with Hydra-PEG(petrafocon A hem-larafilcon A) Hybrid Daily...
Ophthalmic
119d
Cleared
Nov 19, 2014
UltraHealth Hybrid Contact Lens for Keratoconus, UltraHealth Flat Cornea...
Ophthalmic
72d
Cleared
Apr 18, 2012
SYNERGEYES SIH (PETRAFOCON A HEM-LARAFILCON A) HYBRID CONTACT LENS
Ophthalmic
135d
Cleared
May 20, 2009
SYNERGEYES SIG (PETRAFOCON A HEM-LARAFILCON A) HYBRID CONTACT LENS
Ophthalmic
140d
Cleared
May 30, 2008
SYNERGEYES HYBRID CONTACT LENSES - DAILY WEAR, MODELS A, M, KC AND PS
Ophthalmic
49d
Cleared
Mar 05, 2008
SYNERGEYES HYBRID CONTACT LENSES-DAILY WEAR
Ophthalmic
40d
Cleared
Jun 22, 2006
SYNERGEYES (PAFLUFOCON D HEM-IBERFILCON A) HYBRID CONTACT LENSES
Ophthalmic
62d
Cleared
Mar 15, 2006
SYNERGEYES PS HYBRID CONTACT LENS
Ophthalmic
61d