CapsoCloud

Web-based software for managing the CapsoCam Plus procedures used by health care providers, readers, download centers, and upload centers, also providing online video reviewing and…

Registry build 21.09.26

Web-based software for managing the CapsoCam Plus procedures used by health care providers, readers, download centers, and upload centers, also providing online video reviewing and reporting functionalities.

1manufacturer
1catalogue number
6510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Registered in Hubei. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NEZ
Manufacturer City Province Registered as Device types
Ankon Technologies Co., Ltd. Wuhan Hubei Contract manufacturer 2

Record

Regulatory record for CapsoCloud
Listed by CapsoVision, Inc., United States
FDA product code NEZ
Device type System, Imaging, Gastrointestinal, Wireless, Capsule
Device class Class 2
Regulation 21 CFR 876.1300
Establishment Manufacturer
510(k) K192662
Record published 2020-03-02
Record revised 2020-12-10 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for CapsoCloud
Catalogue number Size Status
2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pillcam Given Imaging Ltd. 65
Rapid Given Imaging Ltd. 21
MiroCam Capsule Endoscope System IntroMedic Co., Ltd. 15
PillCam Covidien LP 9
NaviCam Small Bowel Capsule Endoscopy System Ankon Technologies Co., Ltd. 5
System, Imaging, Gastrointestinal, Wireless, Capsule Given Imaging Ltd. 3
PillCam Genius Given Imaging Ltd. 3
AdvanCE Us Endoscopy 2
MiroCam Capusle Endoscope System IntroMedic Co., Ltd. 2
CapsoCam Plus CapsoVision, Inc. 2
CapsoRetrieve CapsoVision, Inc. 2
CapsoView CapsoVision, Inc. 1

Showing 12 of 44. All products under System, Imaging, Gastrointestinal, Wireless, Capsule

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252480 2025-12-19
K242643 2024-12-04
K192662 2020-02-14
K183192 2019-04-19
K161773 2016-10-21
K151635 2016-02-09

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of CapsoCloud
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
CapsoVision, Inc. 510(k) number 2020-02-26 Class II Employee error Ingestible video capsule system has capsule with incorrect capture mode which will not record data when the capsule is ingested by patients. If used, there is a risk of delay of diagnosis and the patient may need to repeat the exam. 82 2021-01-28

Recalls

2 of these are 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 Closed
2019-10-18 Class II Other Capsule Endoscopy System: a defect present in the capsule window may be stressed through the production process and in the final package, which could cause the housing of the capsule to crack and leak when ingested. Fluid from the patient c 1882 2021-01-08
2019-07-03 Class II Process control Possible mis-labeling of the device with incorrect serial number labels which may result in a patient’s misdiagnosis. 44 units 2021-01-28

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