Oasis Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oasis Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SOFT PLUG Extended Duration 180 Tapered Canalicular Plug
17
Total
17
Cleared
0
Denied
Oasis Medical, Inc. has 17 FDA 510(k) cleared ophthalmic devices. Based in Glendora, US.
Last cleared in 2022. Active since 1991.
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 - Oasis Medical, Inc.
17 devices
Cleared
Jun 03, 2022
SOFT PLUG Extended Duration 180 Tapered Canalicular Plug
Ophthalmic
165d
Cleared
Apr 17, 2017
Soft Plug Extended Duration 180 Canalicular Plug
Ophthalmic
237d
Cleared
Aug 26, 2003
DISPOSABLE N-PE MICKROKERATOME BLADES
Ophthalmic
32d
Cleared
Jun 19, 2003
DISPOSABLE M2-PE MICROKERATOME BLADES
Ophthalmic
133d
Cleared
Oct 03, 2002
DISPOSABLE N-PE MICROKERATOME BLADES
Ophthalmic
90d
Cleared
Jun 27, 2002
SOFT PLUG ABSORBABLE PLUG-SA
Ophthalmic
234d
Cleared
Mar 08, 2001
DISPOSABLE CB-PE MICROKERATOME BLADES
Ophthalmic
87d
Cleared
Sep 21, 2000
DISPOSABLE MICROKERATOME BLADES-PE
Ophthalmic
163d
Cleared
Apr 30, 1998
SILICONE PUNCTAL PLUG
Ophthalmic
85d
Cleared
May 22, 1995
POSTERIOR CAPSULE SHIELD
Ophthalmic
90d
Cleared
Feb 27, 1995
OPHTHALMIC SPONGES
Ophthalmic
38d
Cleared
Feb 07, 1995
COLLAGEN INTRACANALICULAR PLUG
Ophthalmic
39d