Medical Device Manufacturer · US , Salt Lake City , UT

Ion Laser Technology - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1991

Total

Cleared

Denied

Ion Laser Technology has 9 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Historical record: 9 cleared submissions from 1991 to 1998. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Ion Laser Technology Filter by specialty or product code using the sidebar.

Ion Laser Technology 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 - Ion Laser Technology

9 devices

1-9 of 9

ACL-5500 PRECISION CURING UNIT (PCU)

General & Plastic Surgery · 84d

Cleared Mar 24, 1995

CL-5500 (UNMODIFIED DEVICE) PRECISION CURING UNIT (PCU) (MODIFIED OPTION)

K950351 · GEX

General & Plastic Surgery · 53d

Cleared Oct 11, 1994

GENESIS 2000

K944206 · GEX

General & Plastic Surgery · 43d

Cleared Oct 11, 1994

GENESIS 2000

K944317 · GEX

General & Plastic Surgery · 43d

Cleared Apr 10, 1992

CARBON DIOXIDE CO2 LASER

K915656 · GEX

General & Plastic Surgery · 114d

Cleared Dec 17, 1991

ILT CO2 SURGICAL LASER FOR ORAL SOFT TISSUE PROCED

K914726 · GEX

General & Plastic Surgery · 57d

Ion Laser Technology - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ion Laser Technology

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