Soflex Contact Lens Industries , Ltd. is one of 25418 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Soflex Contact Lens Industries , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SOFLEX SOFT K (XYLOFILCON A) SOFT (HYDROPHILIC) KERATOCONUS CONTACT LENS FOR DAILY WEAR, ENI-EYE Q TORIC (ACOFILCON) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS FOR DAILY WEAR, ENI-EYE (ACOFILCON) SOFT (HYDROP, SOFT K. AND SOFT K. TORIC (XYLOFICON A) SOFT (HYDROPHILLIC) KERATOCONUS CONTACT LENS FOR DAILY WEAR
6
Total
6
Cleared
0
Denied
Soflex Contact Lens Industries , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 6 cleared submissions from 2001 to 2004. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Soflex Contact Lens Industries , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Soflex Contact Lens Industries , Ltd.
6 devices
Cleared
Jul 30, 2004
SOFLEX SOFT K (XYLOFILCON A) SOFT (HYDROPHILIC) KERATOCONUS CONTACT LENS FOR...
Ophthalmic
252d
Cleared
Jun 06, 2003
ENI-EYE Q TORIC (ACOFILCON) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS FOR...
Ophthalmic
81d
Cleared
May 24, 2002
SOFT K. AND SOFT K. TORIC (XYLOFICON A) SOFT (HYDROPHILLIC) KERATOCONUS...
Ophthalmic
86d
Cleared
Nov 20, 2001
TORIC EYE-Q (XYLOFILCON A) SOFT (HYDROPHILIC) TORIC MULTIFOCAL CONTACT LENS...
Ophthalmic
33d
Cleared
Nov 20, 2001
EYE-Q (XYLOFILCON A) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS FOR DAILY WEAR
Ophthalmic
33d
Cleared
Jul 17, 2001
TORIC LITE LENS
Ophthalmic
84d