Medical Device Manufacturer · US , Irvine , CA

Intra Lase Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1999

Total

Cleared

Denied

Intra Lase Corp. has 9 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 9 cleared submissions from 1999 to 2008. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Intra Lase Corp. Filter by specialty or product code using the sidebar.

Intra Lase Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Intra Lase Corp.

9 devices

1-9 of 9

Cleared Apr 25, 2008

IFS LASER SYSTEM

K073404 · GEX

General & Plastic Surgery · 143d

Cleared Feb 09, 2007

INTRALASE FUSION LASER

K063682 · GEX

General & Plastic Surgery · 60d

Cleared Aug 16, 2006

INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3

K060372 · GEX

General & Plastic Surgery · 184d

Cleared Jul 29, 2005

INTRALASE FS LASER

K041893 · GEX

General & Plastic Surgery · 381d

Cleared Sep 29, 2003

INTRALASE FS LASER

K031960 · GEX

General & Plastic Surgery · 96d

Cleared Feb 27, 2002

PULSION FS LASER KERATOME

K013941 · GEX

General & Plastic Surgery · 90d

Cleared Aug 09, 2001

INTRALASE 600C LASER KERATOME

K002890 · GEX

General & Plastic Surgery · 328d

Cleared Dec 04, 2000

MODIFICATION TO INTRALASE 600C LASER KERATOME

K001211 · GEX

General & Plastic Surgery · 234d

Cleared Dec 17, 1999

INTRALASE 600C LASER KERATOME

K993153 · GEX

General & Plastic Surgery · 87d

Intra Lase Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Intra Lase Corp.

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