MOLEKULE GROUP, INC.

FDA Device Registration & Listing · Lakeland, FL, US · Registration 3019585201

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
3019585201
FEI Number
3019585201
Entity Name
MOLEKULE GROUP, INC.
City/State/Country
Lakeland, FL, US
Establishment Address
4000 N. Combee Rd., Lakeland, FL 33805, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Molekule Group, Inc. (Owner Number: 10072687)
Owner / Operator Contact Address
10455 Riverside Drive, Suite 100, Palm Beach Gardens, FL 33410, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K202339
PMA Number
N/A

All Registered Proprietary Names

Air Pro RX Molekule Air Mini + Molekule Air Mini

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRA Purifier, Air, Ultraviolet, Medical General Hospital Class 2 880.6500 2020-04-30
FRA Purifier, Air, Ultraviolet, Medical General Hospital Class 2 880.6500 2021-02-23

Official Correspondent

Frank Bianco

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Molekule Group, 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 3019585201. Last updated year: 2026. Please use registration number 3019585201 when referencing this establishment in official correspondence.
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