CONAIR LLC.

FDA Device Registration & Listing · STAMFORD, CT, US · Registration 1222304

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
1222304
FEI Number
1000121041
Entity Name
CONAIR LLC.
City/State/Country
STAMFORD, CT, US
Establishment Address
1 CUMMINGS POINT RD., STAMFORD, CT 06902, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Conair LLC. (Owner Number: 2242745)
Owner / Operator Contact Address
1 CUMMINGS POINT RD., --, Stamford, CT 06902, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lumilisse Conair Interplank CONAIR INTERPAK WATER TEST

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect General, Plastic Surgery Class 2 878.4810 2018-01-23
OHT Light Based Over-The-Counter Hair Removal General, Plastic Surgery Class 2 878.4810 2018-01-23
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2014-08-21
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2024-08-14
OLP Over-The-Counter Powered Light Based Laser For Acne General, Plastic Surgery Class 2 878.4810 2024-08-14
JEQ Toothbrush, Powered Dental Class 1 872.6865 1997-02-12
EFS Unit, Oral Irrigation Dental Class 1 872.6510 2004-01-21

Official Correspondent

Stephen Pizzolato

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K192521 Shangdong Huamei Technology Co., Ltd. Intense Pulsed Light Treatment System 2019-12-06
K844318 Pro Pulse, Inc. ORAL IRRIGATION TIP 1984-11-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1222304. Last updated year: 2026. Please use registration number 1222304 when referencing this establishment in official correspondence.
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