Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2182861

FEI Number

2182861

Entity Name

ANTARES PHARMA, INC.

City/State/Country

Minnetonka, MN, US

Establishment Address

12500 Whitewater Drive, Minnetonka, MN 55343, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ANTARES PHARMA, INC. (Owner Number: 2182861)

Owner / Operator Contact Address

12500 Whitewater Drive, Minnetonka, MN 55343, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Xyosted

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NSC	Injector, Pen	General Hospital	Class 2	880.5860	2023-10-12

Official Correspondent

Kristin Schwartzbauer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ANTARES PHARMA, 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 2182861. Last updated year: 2026. Please use registration number 2182861 when referencing this establishment in official correspondence.