NXTSTIM, LLC

FDA Device Registration & Listing · San Diego, CA, US · Registration 3022631685

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
3022631685
FEI Number
3022631685
Entity Name
NXTSTIM, LLC
City/State/Country
San Diego, CA, US
Establishment Address
5362 Sweetwater Trail, San Diego, CA 92130, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
NXTSTIM, INC (Owner Number: 10085260)
Owner / Operator Contact Address
5362 Sweetwater Trail, San Diego, CA 92130, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K192733
PMA Number
N/A

All Registered Proprietary Names

EcoAi

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2023-03-17
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2023-03-17
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2023-03-17

Official Correspondent

Krishnan Chakravarthy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NXTSTIM, INC
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
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21
K033455 Biomedical Life Systems, Inc. ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 2004-01-15
K810593 Medical Devices, Inc. NEUROPAC ULTRA I 1981-03-13
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022631685. Last updated year: 2026. Please use registration number 3022631685 when referencing this establishment in official correspondence.
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