Medical Device Manufacturer · US , San Diego , CA

Clinicon Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1996

Total

Cleared

Denied

Clinicon Corp. has 9 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 9 cleared submissions from 1996 to 2012. Primary specialty: General & Plastic Surgery.

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

Clinicon 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 - Clinicon Corp.

9 devices

1-9 of 9

Cleared Sep 25, 2012

SURELASE CO2 LASER SYSTEM

K121580 · GEX

General & Plastic Surgery · 118d

Cleared Mar 02, 2007

CO2 LASER SYSTEM, MODEL C-LAS

K063698 · GEX

General & Plastic Surgery · 79d

Cleared Mar 26, 2002

CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES

K014236 · GEX

General & Plastic Surgery · 90d

Cleared Feb 11, 2002

CLINICON UNIVERSAL WAVEGUIDE HANDPIECE AND FIBER TIPS

K014048 · GEX

General & Plastic Surgery · 66d

Cleared Sep 08, 1999

SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM

K992472 · GEX

General & Plastic Surgery · 44d

Cleared Dec 11, 1998

SURECAUT DIAMOND LASER KNIFE

K983463 · GEX

General & Plastic Surgery · 71d

Cleared Oct 29, 1997

K970143 · GEX

General & Plastic Surgery · 287d

Cleared Aug 08, 1997

SURESCAN

K964831 · GEX

General & Plastic Surgery · 249d

Cleared Sep 03, 1996

SURESCAN

K962242 · GEX

General & Plastic Surgery · 84d

Clinicon Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Clinicon Corp.

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