Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009595561

FEI Number

3009595561

Entity Name

ASCENT CONSUMER PRODUCTS, INC.

City/State/Country

Melville, NY, US

Establishment Address

105 Baylis Rd, Melville, NY 11747, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Ascent Consumer Products, Inc. (Owner Number: 10040801)

Owner / Operator Contact Address

105 Baylis Road, Melville, NY 11747, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2023-12-14
KCJ	Applicator, Ent	Ear, Nose, Throat	Class 1	874.5220	2016-12-13

Official Correspondent

Matthew Kornberg

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ascent Consumer Products, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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3021011196	E-LINKCARE MEDITECH CO., LTD.	Taizhou Zhejiang, CN
3012896103	SHENZHEN BALINDA TECHNOLOGY CO.,LTD	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009595561. Last updated year: 2026. Please use registration number 3009595561 when referencing this establishment in official correspondence.