ASCENTRON, INC.

FDA Device Registration & Listing · White City, OR, US · Registration 3013069546

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
3013069546
FEI Number
3013069546
Entity Name
ASCENTRON, INC.
City/State/Country
White City, OR, US
Establishment Address
994 Antelope Rd., White City, OR 97503, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Ascentron, Inc. (Owner Number: 10060122)
Owner / Operator Contact Address
994 Antelope Rd., White City, OR 97503, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dynatron Solaris Series (model numbers 709, 708, 706, and 705) Osteoboost D125, D125B

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2019-04-01
IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat Physical Medicine Class 2 890.5300 2019-04-01
LIH Interferential Current Therapy Neurology Class 2 882.5890 2019-04-01
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2019-04-01
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2019-04-01
QZO Wearable Vibration Device For Orthopedic Use Orthopedic Class 2 888.5895 2025-06-23
IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat Physical Medicine Class 2 890.5300 2021-03-31

Official Correspondent

Amanda Brewer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ascentron, 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
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
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04
K964028 Mettler Electronics Corp. SYS STIM 226 1997-02-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013069546. Last updated year: 2026. Please use registration number 3013069546 when referencing this establishment in official correspondence.
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