Organon LLC

FDA Device Registration & Listing · Jersey City, NJ, US · Registration 3017425145

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
3017425145
FEI Number
3017425145
Entity Name
Organon LLC
City/State/Country
Jersey City, NJ, US
Establishment Address
30 Hudson Street, Floor 33, Jersey City, NJ 07302, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Organon LLC (Owner Number: 10077872)
Owner / Operator Contact Address
30 Hudson Street, Floor 33, Jersey City, NJ 07302, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NuvaRing Applicator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HGD Applicator, Vaginal Obstetrics/Gynecology Class 1 884.4520 2024-02-14

Official Correspondent

Suraj Ramachandran

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Organon LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3002806821 N.V. Organon Oss Noord-Brabant, NL

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017425145. Last updated year: 2026. Please use registration number 3017425145 when referencing this establishment in official correspondence.
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