Paragon Vision Sciences - FDA 510(k) Cleared Devices
15
Total
13
Cleared
0
Denied
Paragon Vision Sciences has 13 FDA 510(k) cleared ophthalmic devices. Based in Phoenix, US.
Historical record: 13 cleared submissions from 1994 to 2018.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Paragon Vision Sciences
15 devices
Cleared
Mar 16, 2018
FluoroPerm 30 & Paragon Thin (paflufocon C) RGP contact lenses with Tangible...
Ophthalmic
53d
Cleared
Jun 28, 2012
FLUOROPERM 30 PARAGON HDS FLUOROPERM 60 PARAGON HDS 100 FLUOROPERM 92...
Ophthalmic
87d
Cleared
Jan 27, 2009
HDS HI 1.54
Ophthalmic
126d
Cleared
May 01, 2007
FLUOROPERM 92, 60, 30 AND 151 AND PARAGON HDS, HDS 100 AND THIN RIGID GAS...
Ophthalmic
55d
Cleared
Feb 10, 2006
FLUOROPERM 151 (PAFLUFOCON D) AND PARAGON HDS 100 (PAFLUFOCON D) RIGID GAS...
Ophthalmic
109d
Cleared
Apr 25, 2002
PVS BASIC 2
Ophthalmic
203d
Cleared
Feb 28, 2001
FLUOROPERM 151-OK, PARAGON HDS 100-OK
Ophthalmic
47d
Cleared
Dec 08, 2000
PAFLUFOCON C AND E DAILY CONTACT LENS
Ophthalmic
87d
Cleared
May 22, 2000
SPORTSIGHT GP
Ophthalmic
213d
Cleared
Apr 17, 2000
FLUROPERM 60-OK, PARAGON HDS-OK
Ophthalmic
84d
Cleared
Dec 22, 1999
PARAGON LENS CARRIER
Ophthalmic
68d
Cleared
Dec 22, 1999
PARAGON LENS VIAL
Ophthalmic
68d