MiniX-V

The MiniX-V is a hand-held diagnostic dental x-ray system. It is intended to be used by trained dentists and dental technicians as an extra-oral X-ray source producing diagnostic X-ray…

Registry build 21.09.26

The MiniX-V is a hand-held diagnostic dental x-ray system. It is intended to be used by trained dentists and dental technicians as an extra-oral X-ray source producing diagnostic X-ray images using with intra-oral image receptors. Its use is intended for adults and pediatric subjects both. This device includes a high frequency inverter that changes direct current to alternating current, X-ray tube, electrical protective devices, and other elements. The system helps to get sharp and clear x-ray images, and its low radiation dosage keeps patients and dentists safe from leakage radiation.

8manufacturers in China registered for this device type
1catalogue number
6510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Guangxi (2), Guangdong (2), Zhejiang (2).

Chinese manufacturers registered for FDA product code EHD
Manufacturer City Province Registered as Device types
Guilin Woodpecker Medical Instrument Co., Ltd. Guilin Guangxi Manufacturer 25
Changzhou Sifary Medical Technology Co., Ltd. Changzhou Jiangsu Manufacturer 14
Guangzhou Ajax Medical Equipment Co Ltd Guangzhou Guangdong Manufacturer 13
Guilin Refine Medical Instrument Co., Ltd. Guilin Guangxi Contract manufacturer 7
iRay Imaging Technology (Haining) Limited Haining Zhejiang Contract manufacturer 6
Orich Medical Equipment (Tianjin) Co., Ltd. Tianjin Tianjin Manufacturer 5
Ningbo Runyes Medical Instrument Co., Ltd. Ningbo Zhejiang Contract manufacturer 4
Shenzhen Xpectvision Technology Co., Ltd. Shenzhen Guangdong Repacker / relabeller 4

Record

Regulatory record for MiniX-V
Listed by Digimed Co., Ltd., South Korea
FDA product code EHD
Device type Unit, X-Ray, Extraoral With Timer
Device class Class 2
Regulation 21 CFR 872.1800
Establishment Manufacturer
Record published 2016-11-07
Record revised 2019-04-01 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment atmospheric pressure 80 to 106 KiloPascal; Handling environment humidity 10 to 85 % RH; Handling environment temperature 10 to 35 °C; Storage environment atmospheric pressure 80 to 106 KiloPascal; Storage environment humidity 5 to 90 % RH; Storage environment temperature -20 to 60 °C
Packaging Carton package of 8, carton package of 7, carton package of 6, carton package of 5, carton package of 4, carton package of 3

Catalogue Numbers

Catalogue numbers for MiniX-V
Catalogue number Size Status
1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Midmark Midmark Corporation 148
Midmark Preva IntraOral Dental X-ray System Midmark Corporation 136
Schick AE Sirona Dental, Inc. 53
Midmark Preva 2.0 IntraOral Dental X-ray System Midmark Corporation 46
Xios AE Sirona Dental, Inc. 38
X-Mind unity DE Götzen SRL 26
Midmark Vetpro IntraOral Dental X-ray System Midmark Corporation 26
x-mind dc DE Götzen SRL 17
Owandy-RX DC Owandy Radiology 16
Orthophos XG Sirona Dental Systems Gmbh 10
Schick Elite Sirona Dental, Inc. 10
Phot-X IIs Model 505 Takara Belmont Corporation 10

Showing 12 of 171. All products under Unit, X-Ray, Extraoral With Timer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K221587 2023-03-03
K220579 2022-09-01
K220574 2022-04-22
K181891 2018-08-10
K103600 2011-04-08
K082167 2008-09-26

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2025-06-19 Class II Radiation Control for Health and Safety Act Some DIOX-602 units currently in use within the United States do not meet the minimum SSD requirement of 18 cm. 530

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer