Metro Optics of Austin, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Metro Optics of Austin, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Metro Soft, Silicone Hydrogel Daily Wear Soft Contact Lens (efrofilcon A)
8
Total
8
Cleared
0
Denied
Metro Optics of Austin, Inc. has 8 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Latest FDA clearance: Feb 2024. Active since 1996. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Metro Optics of Austin, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Andre Vision and Device Research as regulatory consultant.
FDA 510(k) Regulatory Record - Metro Optics of Austin, Inc.
8 devices
Cleared
Feb 06, 2024
Metro Soft, Silicone Hydrogel Daily Wear Soft Contact Lens (efrofilcon A)
Ophthalmic
131d
Cleared
Oct 28, 2010
METRO SOFT
Ophthalmic
274d
Cleared
Jul 23, 2008
REVITALEYES, POST-SURGICAL SOFT DAILY WEAR CONTACT LENS (HIOXIFILCON B) CLEAR...
Ophthalmic
149d
Cleared
Aug 01, 2003
SATUREEYES II (ACOFILCON A), (ACOFILCON B) & (TETRAFILCON A) SOFT CONTACT...
Ophthalmic
78d
Cleared
Jun 13, 2000
METROFOCAL TORIC (POLYMACON) SOFT (MULTIFOCAL) DAILY WEAR CONTACT LENS (CLEAR...
Ophthalmic
19d
Cleared
Mar 31, 1999
COMFORTKONE, KERATOCONUS ASPHERIC, RIGID GAS PERMEABLE (RGP), DAILY WEAR...
Ophthalmic
63d
Cleared
Mar 11, 1997
CONTACT LENSES METRO-G 3X (HIOXIFILCON B)
Ophthalmic
95d
Cleared
Nov 20, 1996
METRO FOCAL ASPHERIC (POLYMACON)
Ophthalmic
209d