SOMATICS, LLC

FDA Device Registration & Listing · VENICE, FL, US · Registration 1420295

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
1420295
FEI Number
1420295
Entity Name
SOMATICS, LLC
City/State/Country
VENICE, FL, US
Establishment Address
720 COMMERCE DR UNIT 101, VENICE, FL 34292, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SOMATICS, LLC (Owner Number: 1420295)
Owner / Operator Contact Address
720 Commerce Drive, unit 101, --, Venice, FL 34292, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

EMGD & EMGS EPAD Thymatron

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JXL Block, Bite Neurology Class 2 882.5070 2007-12-19
GXY Electrode, Cutaneous Neurology Class 2 882.1320 2007-12-19
QGH Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder Neurology Class 2 882.5940 2007-12-19

Official Correspondent

Lisa Ventura

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SOMATICS, 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
K070612 Top-Rank Health Care Equipment Co., Ltd. TOP-RANK ADHESIVE ELECTRODE 2007-05-07
K123915 Grass Technologies, an Astro-Med, Inc. Product Gro DE48-PLUS 2013-04-24
K073532 Technomed Europe DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES 2008-05-01
K260363 Ceribell, Inc. Ceribell Brain Monitor Headband 2026-04-03
K091762 Covidien DURA-STICK SELF-ADHESIVE ELECTRODES WITH ALOE 2009-12-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1420295. Last updated year: 2026. Please use registration number 1420295 when referencing this establishment in official correspondence.
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