KUTOL PRODUCTS COMPANY

FDA Device Registration & Listing · Sharonville, OH, US · Registration 1513988

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1513988
FEI Number
1513988
Entity Name
KUTOL PRODUCTS COMPANY
City/State/Country
Sharonville, OH, US
Establishment Address
100 Partnership Way, Sharonville, OH 45241, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Kutol Products Company (Owner Number: 10087900)
Owner / Operator Contact Address
100 Partnership Way, Sharonville, OH 45241, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

M9 ADAPT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EXB Collector, Ostomy Gastroenterology, Urology Class 1 876.5900 2023-04-27

Official Correspondent

Joe Cittadino

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kutol Products Company
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2012 Convatec Inc. 1
Natura Durahesive ConvaTec Moldable Technology Post-Operative /Surgical System (57 mm) Required for application to a patient immediately after ostomy surgery.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1513988. Last updated year: 2026. Please use registration number 1513988 when referencing this establishment in official correspondence.
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