Medical Device Manufacturer · US , Ansonia , CT

Light Sources, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1985

Total

Cleared

Denied

Light Sources, Inc. has 9 FDA 510(k) cleared medical devices. Based in Ansonia, US.

Historical record: 9 cleared submissions from 1985 to 2015. Primary specialty: General & Plastic Surgery.

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

Light Sources, Inc. is one of 4879 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Light Sources, Inc.

9 devices

1-9 of 9

Cleared Dec 17, 2015

UV Lamps for Indoor Tanning Devices

K151370 · LEJ

General & Plastic Surgery · 210d

Cleared Apr 26, 1990

U.V. SUNLAMP 95UF-II

K901324 · FTC

General & Plastic Surgery · 36d

Cleared Mar 28, 1990

FLUORESCENT T12 UVA LAMP

K900649 · FTC

General & Plastic Surgery · 47d

Cleared Mar 27, 1990

U.V. SUNLAMP (U.V. LIGHT, DERMATOLOGIC)

K900693 · FTC

General & Plastic Surgery · 42d

Cleared Sep 28, 1988

U. V. SUNLAMP 95UF-11

K883952 · FTC

General & Plastic Surgery · 9d

Cleared Dec 30, 1987

U.V. SUNLAMP 95 UF-11

K874889 · FTC

General & Plastic Surgery · 29d

Cleared Feb 09, 1987

U.V. SUNLAMP 95UF-11

K870167 · FTC

General & Plastic Surgery · 26d

Cleared Oct 29, 1985

FLUORESCENT T12 UVA TANNING LAMP

K854004 · FTC

General & Plastic Surgery · 29d

Cleared Oct 01, 1985

FLOURESCENT T12 UVA TANNING LAMP

K853545 · FTC

General & Plastic Surgery · 36d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026

Light Sources, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Light Sources, Inc.

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