AB ELECTRONICS

FDA Device Registration & Listing · Danbury, CT, US · Registration 3007661914

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
3007661914
FEI Number
3007661914
Entity Name
AB ELECTRONICS
City/State/Country
Danbury, CT, US
Establishment Address
37 Apple Ridge Rd, Danbury, CT 06810, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
AB Electronics, LLC (Owner Number: 10092504)
Owner / Operator Contact Address
37 Apple Ridge Rd., Danbury, CT 06810, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BioWaveGO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2025-01-15

Official Correspondent

Malisa Diaz-Smith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AB Electronics, 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
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007661914. Last updated year: 2026. Please use registration number 3007661914 when referencing this establishment in official correspondence.
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