Medical Device Manufacturer · US , Mchenry , IL

Kapp Surgical Instrument, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1984

Total

Cleared

Denied

Kapp Surgical Instrument, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Last cleared in 2021. Active since 1984. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Kapp Surgical Instrument, Inc.

9 devices

1-9 of 9

Cleared Jan 28, 2021

Michler-Kapp Cardiovascular Vent Catheter

K200289 · DWF

Cardiovascular · 358d

Cleared Nov 09, 2007

KAPP BARI-RING ENDOSCOPIC MARKER, MODEL K-9536

K072216 · NEU

General & Plastic Surgery · 92d

Cleared Jan 13, 2006

KAPP BARI-RING, MODEL KS-BR-2005

K050384 · NEU

General & Plastic Surgery · 332d

Cleared Aug 08, 2005

MONDEAL RADIUS HO SYSTEM, MODEL KS-MR-2005

K050655 · HRS

Orthopedic · 147d

Cleared Aug 08, 2005

MONDEAL CONTOUR HO SYSTEM

K050657 · HRS

Orthopedic · 147d

Cleared Jul 28, 2004

KAPP CUSTOM ULNAR HEAD WRIST IMPLANT

K033930 · KXE

Orthopedic · 223d

Cleared Aug 29, 2003

KAPP CUSTOM RADIAL HEAD ELBOW IMPLANT

K030237 · KWI

Orthopedic · 218d

Cleared Nov 08, 1984

COSGROVE MITRAL VALVE RETRACTOR

K844177 · GAD

General & Plastic Surgery · 14d

Kapp Surgical Instrument, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Kapp Surgical Instrument, Inc.

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