Medical Device Manufacturer · US , Mchenry , IL

Med-Tool, Inc. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1984

Total

Cleared

Denied

Med-Tool, Inc. has 28 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.

Historical record: 28 cleared submissions from 1984 to 1987.

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

Med-Tool, 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 - Med-Tool, Inc.

28 devices

1-12 of 28

Cleared Nov 23, 1987

PIN PUNCH

K874356 · LRY

General & Plastic Surgery · 31d

Cleared Nov 23, 1987

TAPERED PUNCH

K874357 · LRY

General & Plastic Surgery · 31d

General & Plastic Surgery · 34d

Cleared Jul 16, 1987

VICE OR BENCH VICE

K872385 · LSA

General & Plastic Surgery · 27d

Cleared Jul 16, 1987

STANDARD SCREW DRIVER

K872387 · LRZ

General & Plastic Surgery · 27d

Cleared Jul 15, 1987

PRECISION SCREW DRIVER SET

K872389 · HXX

Orthopedic · 26d

Cleared Jul 02, 1987

SIDE CUTTING PARALLEL ACTION PLIERS

K872384 · HTC

General & Plastic Surgery · 13d

Cleared Jul 02, 1987

C CLAMP

K872386 · HXD

General & Plastic Surgery · 13d

Cleared Oct 30, 1986

SLOTTED PUNCH

K864017

General & Plastic Surgery · 15d

Cleared Oct 30, 1986

HACKSAW

K864018

General & Plastic Surgery · 15d

Med-Tool, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Med-Tool, Inc.

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