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Kapp Surgical Instrument, Inc.

US

Last updated September 17, 2026

About

KAPP SURGICAL INSTRUMENT INC. Worldwide Sales and Manufacturing Services Learn how our custom instrument design service works. Learn more >> Instruments, implants, specialty sterile products. Shop our complete range of products, purchase bulk quantities for discounts

From the manufacturer's own website. Source

Information

Country
US
Address
4919 WARRENSVILLE CENTER RD., Bedford Heights, OH, 44128
LinkedIn
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Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
1522875
DUNS Number
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Catalogue (126)

Page 2 of 3
DeviceModel / ReferenceRegistriesClassStatus
Seitz Solution Radial Head KCSI-824
FDA UDI
Class IIActive
Seitz Solution Radial Head KCSI-519
FDA UDI
Class IIActive
Coned Heparin Needles KS-4007-7
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7000-L
FDA UDI
Class IActive
Seitz Solution Radial Head KCW-71
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-2014
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7001-G
FDA UDI
Class IActive
Seitz Solution Radial Head KCW-72
FDA UDI
Class IIActive
Adult Renal Clamps – Left KS-2001
FDA UDI
Class IIActive
Baby Renal Clamp – Right KS-1002
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-2315
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-2012
FDA UDI
Class IIActive
Seitz Solution Radial Head KCW-81
FDA UDI
Class IIActive
Modified Javid Clamps KS-5004
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-1811
FDA UDI
Class IIActive
Vasectomy Instruments K-9554
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7001-M
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7101-9
FDA UDI
Class IActive
Seitz Solution Radial Head KCW-92
FDA UDI
Class IIActive
Coned Heparin Needles KS-4003-4
FDA UDI
Class IActive
Coned Heparin Needles KS-4005-7
FDA UDI
Class IActive
Coned Heparin Needles KS-4006-7
FDA UDI
Class IActive
Adult Renal Clamps – Right KS-2002
FDA UDI
Class IIActive
Vessel Retractors K-9780
FDA UDI
Class IActive
Seitz Solution Unlar Head KCUH-1515
FDA UDI
Class IIActive
Seitz Solution Unlar Head KCUC-4854
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-1809
FDA UDI
Class IIActive
Bulldog Clamp KS-3008
FDA UDI
Class IIActive
Seitz Solution Unlar Head KCUC-4876
FDA UDI
Class IIActive
Seitz Solution Radial Head KCSI-621
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-2010
FDA UDI
Class IIActive
Coned Heparin Needles KS-4008
FDA UDI
Class IActive
Seitz Solution Radial Head KCW-52
FDA UDI
Class IIActive
Seitz Solution Radial Head KCW-82
FDA UDI
Class IIActive
Loop Aorta Clamp KS-7700
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-2614
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7103-L
FDA UDI
Class IActive
Ankeney Sternal Retractor K-9779
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7103
FDA UDI
Class IActive
Martinez Clamp KS-9999MCL
FDA UDI
Class IIActive
Seitz Solution Unlar Head KCS-51
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7101-10
FDA UDI
Class IActive
Hardy Retractor K-9445
FDA UDI
Class IActive
Coned Heparin Needles KS-4003-7
FDA UDI
Class IActive
Seitz Solution Radial Head KCW-91
FDA UDI
Class IIActive
Bulldog Clamp KS-3007
FDA UDI
Class IIActive
Lateral Tibia Retractor - Left Left
FDA UDI
Class IActive
Modified Javid Clamps KS-5001
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7001-A
FDA UDI
Class IActive
Coned Heparin Needles KS-4001-4
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
May 24, 2011Z-2753-2011—terminated

During an FDA Inspection on 3/21/11 - 3/22/11 at Kapp Surgical an uncontrolled instruction for use was discovered which contained sterilization parameters which differed from the instructions contained in the device master record. Kapp Surgical decided to conduct the recall because we cannot be sure that incorrect instructions were not shipped.

Mar 5, 2008Z-0068-2012—terminated

A portion of the labeled expiration date is missing. The expiration date on approximately half of the pouch labels distributed are missing the last digit of the year of expiration. However, the shelf box containing the pouches is labeled correctly.