PreXion3D Explorer PRO

Catalogue number P03A, listed by Prexion Corporation, Japan, under X-Ray, Tomography, Computed, Dental. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
9510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (2), Guangdong (1), Zhejiang (1).

Chinese manufacturers registered for FDA product code OAS
Manufacturer City Province Registered as Device types
Changzhou Sifary Medical Technology Co., Ltd. Changzhou Jiangsu Manufacturer 14
Fussen Technology Co., Ltd. Shenzhen Guangdong Manufacturer 3
Yian Medical Technology (Haining) Co., Ltd. Jiaxing Zhejiang Specification developer 1
Changzhou Finno Medical Technology Co., Ltd. Changzhou Jiangsu Manufacturer 1

Record

Regulatory record for PreXion3D Explorer PRO
Listed by Prexion Corporation, Japan
FDA product code OAS
Device type X-Ray, Tomography, Computed, Dental
Device class Class 2
Regulation 21 CFR 892.1750
Record published 2022-06-28
Record revised 2024-12-30 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for PreXion3D Explorer PRO
Catalogue number Size Status
P03A In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rayscan RAY Co., Ltd., 52
Rayscan Studio RAY Co., Ltd., 21
Dental CT Scanner AXR Alliage S/A Indústrias Médico Odontológica 15
PaX-i3D Green Vatech Co., Ltd. 14
Orthopantomograph™ OP 3D Palodex Group OY 11
Sleeve for extraoral X-Ray devices Sirona Dental Systems Gmbh 11
SXR / Saevo Alliage S/A Indústrias Médico Odontológica 11
X-Mind trium DE Götzen SRL 10
Genoray Genoray Co., Ltd. 9
Rayscan α-Expert3D RAY Co., Ltd., 9
Orthophos SL Sirona Dental Systems Gmbh 9
Orthophos XG Sirona Dental Systems Gmbh 9

Showing 12 of 110. All products under X-Ray, Tomography, Computed, Dental

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K232166 2023-09-08
K222150 2023-01-12
K221525 2022-07-22
K203784 2021-02-23
K193329 2020-04-09
K190320 2019-04-15
K181983 2018-08-17
K173878 2018-01-19
K161881 2016-10-03

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