OSTOMY ASSIST

FDA Device Registration & Listing · Clayton, MO, US · Registration 3042024502

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
3042024502
FEI Number
3042024502
Entity Name
OSTOMY ASSIST
City/State/Country
Clayton, MO, US
Establishment Address
7733 Forsyth Blvd Ofc 1156, Clayton, MO 63105, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Ostomy Assist (Owner Number: 10094260)
Owner / Operator Contact Address
7733 Forsyth Blvd, office 1156, Clayton, MO 63105, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Ostomy Asisst

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EXB Collector, Ostomy Gastroenterology, Urology Class 1 876.5900 2025-11-20

Official Correspondent

Andrew Kelly

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ostomy Assist
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 3042024502. Last updated year: 2026. Please use registration number 3042024502 when referencing this establishment in official correspondence.
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