PDO MAX

FDA Device Registration & Listing · Liverpool, NY, US · Registration 3015289316

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
3015289316
FEI Number
3015289316
Entity Name
PDO MAX
City/State/Country
Liverpool, NY, US
Establishment Address
4971 Bear Road, Suite 102, Liverpool, NY 13088, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
PDO MAX (Owner Number: 10060757)
Owner / Operator Contact Address
4971 Bear Road, Liverpool, NY 13088, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lumenvy Skincare Valluxia LED Mask REJUVN8 Threads PDO MAXX Threads PDO Max Dual Needle PDO Max Cannulas

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLP Over-The-Counter Powered Light Based Laser For Acne General, Plastic Surgery Class 2 878.4810 2025-07-23
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2025-07-23
NEW Suture, Surgical, Absorbable, Polydioxanone General, Plastic Surgery Class 2 878.4840 2019-06-20
NEW Suture, Surgical, Absorbable, Polydioxanone General, Plastic Surgery Class 2 878.4840 2022-01-10
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2019-07-23

Official Correspondent

Juliana Koval

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PDO MAX
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
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015289316. Last updated year: 2026. Please use registration number 3015289316 when referencing this establishment in official correspondence.
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