FDA.reportPublic FDA data

KAPP SURGICAL INSTRUMENT, INC.

Matched from indexed company URL: Kapp Surgical Instrument Co.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
15228751522875KAPP SURGICAL INSTRUMENT, INC.1N2026-01-014919 WARRENSVILLE CENTER RD. Bedford Heights OH US 44128

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
B033K9536N0Bari Ring - Nitinol Version216-587-4400info@kappsurgical.com
B033KS400140Coned Heparin Needles - Coned Heparin Needles – Size 01 - 4in216-587-4400info@kappsurgical.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
318041257908707K200289Michler-Kapp Cardiovascular Vent CatheterDWF2021-01-28
318042035811837K033930KAPP CUSTOM ULNAR HEAD WRIST IMPLANTKXE2004-07-28
318042002883937K030237KAPP CUSTOM RADIAL HEAD ELBOW IMPLANTKWI2003-08-29
318041042035183
318041205885793
318041267844801
318041279783086
318041288124936
318041350885087
318041357407828
318041363953419
318041364397323
318041393653571
318041414945813
318041415982891
318041471755934
318041704270042
318041777539651
318041792160396
318041840790192
318041922632891
318041945357602
318041990615738

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DWF12021-01-28
KXE12004-07-28
KWI12003-08-29

PMN#

GUDID#

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