LUMICELL, INC

FDA Device Registration & Listing · Waltham, MA, US · Registration 3017718237

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
3017718237
FEI Number
3017718237
Entity Name
LUMICELL, INC
City/State/Country
Waltham, MA, US
Establishment Address
307 Waverly Oaks Rd Ste 309, Waltham, MA 02452, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Lumicell, Inc (Owner Number: 10090701)
Owner / Operator Contact Address
307 Waverly Oaks Rd, Ste 309, Waltham, MA 02452, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P230014

All Registered Proprietary Names

Lumicell Direct Visualization System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SAW Fluorescence Imaging For Breast Cancer Detection Unknown Class 3 N/A 2024-04-30

Official Correspondent

Jorge Ferrer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lumicell, Inc
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 3017718237. Last updated year: 2026. Please use registration number 3017718237 when referencing this establishment in official correspondence.
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