CATH DRY GLOBAL, INC

FDA Device Registration & Listing · Los Angeles, CA, US · Registration 3013613028

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
3013613028
FEI Number
3013613028
Entity Name
CATH DRY GLOBAL, INC
City/State/Country
Los Angeles, CA, US
Establishment Address
1243 North Hoover Street, Los Angeles, CA 90029, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Cath Dry, Inc (Owner Number: 10085908)
Owner / Operator Contact Address
1243 North Hoover Street, Los Angeles, CA 90029, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMK Device, Intravascular Catheter Securement General Hospital Class 1 880.5210 2022-09-04

Official Correspondent

Pascal Dabel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cath Dry, Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013613028. Last updated year: 2026. Please use registration number 3013613028 when referencing this establishment in official correspondence.
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