Medical Device Manufacturer · US , Manchester , VT

The Orvis Co., Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

The Orvis Co., Inc. has 9 FDA 510(k) cleared medical devices. Based in Manchester, US.

Historical record: 9 cleared submissions from 1994 to 1995. Primary specialty: Ophthalmic.

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

The Orvis Co., 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 - The Orvis Co., Inc.

9 devices

1-9 of 9

Cleared Mar 02, 1995

ORVIS KEY WEST SUNGLASSES

K950609 · HQY

Ophthalmic · 20d

Cleared Aug 04, 1994

ORVIS DRIVING GLASSES

K943161 · HQY

Ophthalmic · 34d

Cleared Aug 02, 1994

ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS

K942951 · HQY

Ophthalmic · 40d

Cleared Aug 02, 1994

ORVIS POLARIZED BI-FOCALS

K943131 · HQY

Ophthalmic · 34d

Cleared Jul 25, 1994

ORVIS WORLD FINEST POLARIZED CLIP ONS

ORVIS RIVER GUIDE GLASSES

K940292 · HQY

Ophthalmic · 62d

Cleared Mar 24, 1994

ORVIS MARQUESAS FISHING GLASSES

K940354 · HQY

Ophthalmic · 58d

The Orvis Co., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - The Orvis Co., Inc.

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