Permeable Technologies, Inc. is one of 22925 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Permeable Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIFESTYLE 4-VUE (POLYMACON) HYDROPHILIC MULTIFOCAL CONTACT LENS FOR DAILY WEAR, LIFESTYLE FREQUENCY PROGRESSIVE (METHAFILCON A) MULTIFOCAL HYDROPHILIC CONTACT LENSES FOR DAILY WEAR, LIFESTYLE GP (TELEFOCON B) RIGID GAS PERMEABLE MULTIFOCAL CONTACT LENS FOR DAILY WEAR
7
Total
7
Cleared
0
Denied
Permeable Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Morganville, US.
Historical record: 7 cleared submissions from 1994 to 1997. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Permeable Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Permeable Technologies, Inc.
7 devices
Cleared
Mar 11, 1997
LIFESTYLE 4-VUE (POLYMACON) HYDROPHILIC MULTIFOCAL CONTACT LENS FOR DAILY WEAR
Ophthalmic
221d
Cleared
Nov 29, 1996
LIFESTYLE FREQUENCY PROGRESSIVE (METHAFILCON A) MULTIFOCAL HYDROPHILIC...
Ophthalmic
119d
Cleared
Nov 20, 1996
LIFESTYLE GP (TELEFOCON B) RIGID GAS PERMEABLE MULTIFOCAL CONTACT LENS FOR...
Ophthalmic
110d
Cleared
Nov 17, 1995
LIFESTYLE 55 (OCUFILCON D) HYDROPHILIC CONTACT LENS LIFESTYLE FREQUENCY 55...
Ophthalmic
207d
Cleared
Feb 07, 1995
LIFESTYLE 55 (METHAFILCON A) SOFT HYDROPHILIC CONTACT LENS
Ophthalmic
61d
Cleared
Feb 07, 1995
LIFESTYLE 4-VUE(TM) (POLYMACON) HYDROPHILIC CONTACT LENS
Ophthalmic
14d
Cleared
Sep 08, 1994
LIFESTYLE MULTIVUE-S (POLYMACON) SOFT HYDROPHILIC CONTACT LENS
Ophthalmic
106d