DISTRON CORPORATION

FDA Device Registration & Listing · Attleboro Falls, MA, US · Registration 3006621944

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
3006621944
FEI Number
3006621944
Entity Name
DISTRON CORPORATION
City/State/Country
Attleboro Falls, MA, US
Establishment Address
87 John L Dietsch Sq, Attleboro Falls, MA 02763, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Distron Corporation (Owner Number: 10048403)
Owner / Operator Contact Address
87 John L. Dietsch Square, Attleboro Falls, MA 02763, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BioWavePRO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LIH Interferential Current Therapy Neurology Class 2 882.5890 2023-11-20

Official Correspondent

Jason Little

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Distron Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006621944. Last updated year: 2026. Please use registration number 3006621944 when referencing this establishment in official correspondence.
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