ABENA NORTH AMERICA, INC.

FDA Device Registration & Listing · Oceanside, CA, US · Registration 3010048541

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
3010048541
FEI Number
3010048541
Entity Name
ABENA NORTH AMERICA, INC.
City/State/Country
Oceanside, CA, US
Establishment Address
1291 Rocky Point Dr, Suite 101, Oceanside, CA 92056, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Abena North America, Inc. (Owner Number: 10043079)
Owner / Operator Contact Address
1291 Rocky Point Dr, Suite 101, Oceanside, CA 92056, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Delta-Form Abri-Man Abri-Flex Abri-Form Delta-Flex Abena Boost Abri-San Abena Light Abena Man Abena Pants

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2020-02-12

Official Correspondent

Nick Morganti

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Abena North America, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010048541. Last updated year: 2026. Please use registration number 3010048541 when referencing this establishment in official correspondence.
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