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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
—
Facebook
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Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
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FDA FEI Number
1522875
DUNS Number
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Catalogue (126)

Page 1 of 3
DeviceModel / ReferenceRegistriesClassStatus
Coned Heparin Needles KS-4007-4
FDA UDI
Class IActive
Martinez Clamp KS-9999MCR
FDA UDI
Class IIActive
Bulldog Clamp KS-3004
FDA UDI
Class IIActive
Coned Heparin Needles KS-4004-4
FDA UDI
Class IActive
Seitz Solution Radial Head KCHI-1813
FDA UDI
Class IIActive
Seitz Solution Unlar Head KCS-72
FDA UDI
Class IIActive
Yasargil Bulldog Clamp KS-9975
FDA UDI
Class IIActive
Rosenkranz Pediatric Open Heart Retractor K-217
FDA UDI
Class IActive
Bulldog Clamp KS-3002
FDA UDI
Class IIActive
Coned Heparin Needles KS-4002-7
FDA UDI
Class IActive
Baby Renal Clamp – Left KS-1001
FDA UDI
Class IIActive
Seitz Solution Radial Head KCSI-722
FDA UDI
Class IIActive
Vasectomy Instruments K-9490
FDA UDI
Class IActive
Seitz Solution Unlar Head KCUS-5276
FDA UDI
Class IIActive
Rosenkranz Pediatric Open Heart Retractor K-216
FDA UDI
Class IActive
Seitz Solution Unlar Head KCUH-1314
FDA UDI
Class IIActive
Bulldog Clamp KS-3006
FDA UDI
Class IIActive
Seitz Solution Radial Head KCW-62
FDA UDI
Class IIActive
Seitz Solution Radial Head Implant System 18 x 9mm Radial Head KCHI-1809
FDA UDI
Class IIActive
Seitz Solution Unlar Head KCS-61
FDA UDI
Class IIActive
Vasectomy Instruments K-9489
FDA UDI
Class IActive
Seitz Solution Radial Head KCHI-2612
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7111-A
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7107-2S
FDA UDI
Class IActive
Seitz Solution Radial Head Implant System 18 x 11mm Radial Head KCHI-1811
FDA UDI
Class IIActive
Coned Heparin Needles KS-4001-7
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7000-S
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7101-8
FDA UDI
Class IActive
Coned Heparin Needles KS-4006-4
FDA UDI
Class IActive
Bulldog Clamp KS-3001
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7001
FDA UDI
Class IActive
Seitz Solution Unlar Head KCS-52
FDA UDI
Class IIActive
Seitz Solution Unlar Head KCS-71
FDA UDI
Class IIActive
Seitz Solution Radial Head KCHI-2311
FDA UDI
Class IIActive
Loop Aorta Clamp KS-7700XL
FDA UDI
Class IIActive
Bulldog Clamp KS-3005
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7107-2L
FDA UDI
Class IActive
Seitz Solution Radial Head KCSI-925
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7103-R
FDA UDI
Class IActive
Seitz Solution Radial Head KCW-51
FDA UDI
Class IIActive
Coned Heparin Needles KS-4002-4
FDA UDI
Class IActive
Modified Javid Clamps KS-5003
FDA UDI
Class IIActive
Cosgrove Valve Retractor System KS-7103-S
FDA UDI
Class IActive
Knee Retractor Medial Knee Retractor
FDA UDI
Class IActive
Cosgrove Valve Retractor System KS-7002
FDA UDI
Class IActive
Bari Ring Nitinol Version
FDA UDI
Class IIUnknown
Modified Javid Clamps KS-5005
FDA UDI
Class IIActive
Coned Heparin Needles KS-4004-7
FDA UDI
Class IActive
Coned Heparin Needles KS-4005-4
FDA UDI
Class IActive
Seitz Solution Unlar Head KCUS-5254
FDA UDI
Class IIActive

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.