Medical Device Manufacturer · US , Mchenry , IL

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

19 submissions · 19 cleared · Since 1984

Total

Cleared

Denied

Woodlyn, Inc. has 19 FDA 510(k) cleared ophthalmic devices. Based in Mchenry, US.

Historical record: 19 cleared submissions from 1984 to 1993.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

Woodlyn, Inc. 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 - Woodlyn, Inc.

19 devices

1-12 of 19

Cleared Jun 25, 1993

WOODLYN OPERATION MICROSCOPE

K931303 · FSO

General & Plastic Surgery · 102d

Cleared Jul 30, 1992

WOODLYN CLASSIC LENSMETER

K920861 · HLM

Ophthalmic · 156d

Cleared Feb 21, 1990

WOODLYN SLIT LAMP MODEL HR-1

K900476 · HJO

Ophthalmic · 20d

Cleared Feb 21, 1990

WOODLYN CLASSIC SLIT LAMP MODEL SMM

K900477 · HJO

Ophthalmic · 20d

Cleared Feb 21, 1990

WOODLYN FULL APERTURE TRIAL LENS SET

K900478 · HPC

Ophthalmic · 20d

Cleared May 17, 1989

WOODLYN OPHTHALMIC PROJECTOR

K890992 · HOS

Ophthalmic · 79d

Cleared Dec 23, 1987

WOODLYN CLASSIC REFRACTOR, PHOROPTOR

K874900 · HKN

Ophthalmic · 22d

Cleared Dec 11, 1984

WOODLYN CLASSIC CATARACT ACUITY TEST

K843812 · HLI

Ophthalmic · 74d

Cleared Aug 07, 1984

WOODLYN CLASSIC SLIT LAMP HSSL-CL

K841761 · HLI

Ophthalmic · 102d

Cleared Aug 07, 1984

WOODLYN CLASSIC JAVAL OPHTHALMOMETER

K841764 · HLI

Ophthalmic · 102d

Cleared Aug 07, 1984

WOODLYN STANDARD SLIT LAMP HSSL-ST

K841765 · HLQ

Ophthalmic · 102d

Cleared Aug 07, 1984

WOODLYN CLASSIC KERATOMETER

K841767 · HLI

Ophthalmic · 102d

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

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

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