Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011965331

FEI Number

3011965331

Entity Name

Nordic Pharma, Inc.

City/State/Country

Berwyn, PA, US

Establishment Address

1205 Westlakes Drive, Suite 275, Berwyn, PA 19312, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Amring Pharmaceuticals Inc. (Owner Number: 10056388)

Owner / Operator Contact Address

1205 Westlakes Drive, Suite 275, Berwyn, PA 19312, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K222164

PMA Number

N/A

All Registered Proprietary Names

LACRIFILL® Canalicular Gel

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LZU	Plug, Punctum	Unknown	Class U	N/A	2024-04-02

Official Correspondent

Melissa Goodhead

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Amring Pharmaceuticals 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 3011965331. Last updated year: 2026. Please use registration number 3011965331 when referencing this establishment in official correspondence.