DENTIMAX, INC

FDA Device Registration & Listing · Mesa, AZ, US · Registration 3007515144

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
3007515144
FEI Number
3007515144
Entity Name
DENTIMAX, INC
City/State/Country
Mesa, AZ, US
Establishment Address
4115 E Valley Auto Dr, Suite 101, Mesa, AZ 85206, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
DentiMax LLC / Arnett (Owner Number: 10030840)
Owner / Operator Contact Address
4115 E. Valley Auto Drive, Suite 101, Mesa, AZ 85206, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K220556
PMA Number
N/A

All Registered Proprietary Names

OpenSensor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUH System, X-Ray, Extraoral Source, Digital Dental Class 2 872.1800 2022-11-29

Official Correspondent

David Arnett

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DentiMax LLC / Arnett
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
K221008 Shanghai Handy Medical Equipment Co., Ltd. HDR Sensor- HDR361 (Size 1), HDR Sensor- HDR461 (Size 2) 2022-06-22
K160788 Ray Co., Ltd. RIOScan (RPS500) 2016-04-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007515144. Last updated year: 2026. Please use registration number 3007515144 when referencing this establishment in official correspondence.
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