Medical Device Manufacturer · US , Malibu , CA

Iop, Inc. - FDA 510(k) Cleared Devices

9 submissions · 8 cleared · Since 1989

Recent clearances: SUTUREGROOVE, MOA BONE / M-SPHERE

Total

Cleared

Denied

Iop, Inc. has 8 FDA 510(k) cleared medical devices. Based in Malibu, US.

Historical record: 8 cleared submissions from 1989 to 2009. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Iop, Inc. Filter by specialty or product code using the sidebar.

Iop, Inc. is one of 12238 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Iop, Inc.

9 devices

1-9 of 9

Cleared May 08, 2009

KERASYS BIOENGINEERED LAMELLAR PATCH GRAFT

SURGISIS OCULAR GRAFT

K053622 · NXM

Ophthalmic · 77d

Cleared Aug 13, 2001

OSMED TISSUE EXPANDER

K010852 · NFM

Ophthalmic · 145d

Cleared Feb 22, 2001

SUTUREGROOVE WEIGHT SIZING SET

MODIFIED MOLTENO(TM) IMPLANTS

Iop, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Iop, Inc.

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