Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004541026

FEI Number

3004541026

Entity Name

SANOSTEC CORP

City/State/Country

BEVERLY, MA, US

Establishment Address

61 Lakeshore Ave, BEVERLY, MA 01915, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

SANOSTEC CORP (Owner Number: 9062935)

Owner / Operator Contact Address

61 Lakeshore Ave, PO BOX 5650, Beverly, MA 01915, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NOSE CONES SINUS CONES MAX-AIR

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LWF	Dilator, Nasal	Ear, Nose, Throat	Class 1	874.3900	2004-04-20

Official Correspondent

LOUISE MACDONALD

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SANOSTEC CORP

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 3004541026. Last updated year: 2026. Please use registration number 3004541026 when referencing this establishment in official correspondence.