Kavo 3d Exam™ Imaging System

Dental CBCT

Registry build 21.09.26
10manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Guangdong (2), Shanghai (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MUH
Manufacturer City Province Registered as Device types
iRay Imaging Technology Taicang Limited Taicang Jiangsu Contract manufacturer 3
Guilin Woodpecker Medical Instrument Co., Ltd. Guilin Guangxi Manufacturer 25
Changzhou Sifary Medical Technology Co., Ltd. Changzhou Jiangsu Manufacturer 14
Jiangsu Dynamic Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 12
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
iRay Group Shanghai Shanghai Specification developer 4
Fussen Technology Co., Ltd. Shenzhen Guangdong Manufacturer 3
Shanghai Handy Medical Equipment Co., Ltd. Shanghai Shanghai Manufacturer 2

Record

Regulatory record for Kavo 3D eXam™ imaging system
Listed by Dental Imaging Technologies Corporation, United States
FDA product code MUH
Device type System, X-Ray, Extraoral Source, Digital
Device class Class 2
Regulation 21 CFR 872.1800
Establishment Complaint-file establishment, Manufacturer
510(k) K061284
Record published 2016-09-24
Record revised 2025-06-18 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment temperature 10 to 35 °C
Distribution end date 2024-12-31

Catalogue Numbers

Catalogue numbers for Kavo 3D eXam™ imaging system
Catalogue number Size Status
0.830.0000 Withdrawn
0.830.8000 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Schick Elite Sirona Dental, Inc. 38
Schick Wifi Sirona Dental, Inc. 31
Midmark Intraoral Digital Sensor Midmark Corporation 26
Xios XG Wifi Sirona Dental, Inc. 25
Midmark OptiMax Digital Sensor System Midmark Corporation 24
Gendex GXS-700™ intraoral sensor Gendex Corp. 19
Genoray Genoray Co., Ltd. 14
X-Mind trium DE Götzen SRL 12
X-Mind optima 3D DE Götzen SRL 12
Dexis Titanium Sensor Kit Dental Imaging Technologies Corporation 11
Xios XG Select Sirona Dental, Inc. 11
Planmeca ProMax Planmeca Oy 11

Showing 12 of 279. All products under System, X-Ray, Extraoral Source, Digital

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233053 2023-11-21

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Kavo 3D eXam™ imaging system
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Dental Imaging Technologies Corporation 510(k) number 2009-01-08 Not classified Nonconforming Material/Component faulty calibration 24 units 2009-06-04
Dental Imaging Technologies Corporation 510(k) number 2008-03-19 Not classified Error in labeling Incorrect scatter information in the manual. 1203 units 2009-05-05

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