DANELLI OCULAR CREATIONS LLC

FDA Device Registration & Listing · Mishawaka, IN, US · Registration 3018034305

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
3018034305
FEI Number
3018034305
Entity Name
DANELLI OCULAR CREATIONS LLC
City/State/Country
Mishawaka, IN, US
Establishment Address
230 East day Road, Suite 100, Mishawaka, IN 46545, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
DANELLI OCULAR CREATIONS LLC (Owner Number: 10080572)
Owner / Operator Contact Address
230 East day Road, Suite 100, Mishawaka, IN 46545, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MYBOCLEAN Daily Eyelid Cleansing Brush Danelli Brush

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GED Brush, Dermabrasion, Manual General, Plastic Surgery Class 1 878.4800 2021-02-10

Official Correspondent

Bryan Minelli

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DANELLI OCULAR CREATIONS LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018034305. Last updated year: 2026. Please use registration number 3018034305 when referencing this establishment in official correspondence.
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