Medical Device Manufacturer · US , Glendora , CA

Oasis Medical, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1991

Total

Cleared

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) cleared devices by Oasis Medical, Inc.

17 devices

1-12 of 17

Cleared Jun 03, 2022

SOFT PLUG Extended Duration 180 Tapered Canalicular Plug

K213988 · LZU

Ophthalmic · 165d

Cleared Apr 17, 2017

Soft Plug Extended Duration 180 Canalicular Plug

K162361 · LZU

Ophthalmic · 237d

Cleared Aug 26, 2003

DISPOSABLE N-PE MICKROKERATOME BLADES

K032297 · HNO

Ophthalmic · 32d

Cleared Jun 19, 2003

DISPOSABLE M2-PE MICROKERATOME BLADES

K030401 · HNO

Ophthalmic · 133d

Cleared Oct 03, 2002

DISPOSABLE N-PE MICROKERATOME BLADES

K022205 · HNO

Ophthalmic · 90d

Cleared Jun 27, 2002

SOFT PLUG ABSORBABLE PLUG-SA

K013613 · LZU

Ophthalmic · 234d

Cleared Mar 08, 2001

DISPOSABLE CB-PE MICROKERATOME BLADES

K003820 · HNO

Ophthalmic · 87d

Cleared Sep 21, 2000

DISPOSABLE MICROKERATOME BLADES-PE

K001176 · HNO

Ophthalmic · 163d

Cleared Apr 30, 1998

SILICONE PUNCTAL PLUG

K980437 · LZU

Ophthalmic · 85d

Cleared May 22, 1995

POSTERIOR CAPSULE SHIELD

COLLAGEN INTRACANALICULAR PLUG

K946357 · LZU

Ophthalmic · 39d

Oasis Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Oasis Medical, Inc.

Filters