Pillcam

PillCam (TM) Desktop Software v9.7 Upgrade

Registry build 21.09.26
1manufacturer
65catalogue numbers in this listing
19510(k) clearances naming this product code
2recalls 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 Pillcam
Listed by Given Imaging Ltd., Israel
FDA product code NEZ
Device type System, Imaging, Gastrointestinal, Wireless, Capsule
Device class Class 2
Regulation 21 CFR 876.1300
Establishment Manufacturer
510(k) K240276
Record published 2017-02-01
Record revised 2024-11-15 (version 15)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Over the counter Yes
Label carries lot or batch number, expiry date, manufacturing date, serial number
Storage Storage environment temperature 0 to 25 °C; Handling environment temperature 20 to 40 °C
Distribution end date 2021-03-31

Catalogue Numbers

Catalogue numbers for Pillcam
Catalogue number Size Per pack Status
FGS-0619 In distribution
FGS-0584 In distribution
FGS-0214 In distribution
FGS-0637 In distribution
FGS-0581 In distribution
FGS-0803 In distribution
FGS-0586 10 In distribution
FGS-0499 10 In distribution
FGS-0509 In distribution
RFB-0590 In distribution
FGS-0154 In distribution
FGS-0802 In distribution
FGS-0664 In distribution
FGS-0605 In distribution
FGS-0666 5 In distribution
FGS-0502 5 In distribution
FGS-0452 5 In distribution
FGS-0395 5 In distribution
FGS-0569 In distribution
FGS-0482 In distribution
FGS-0453 10 In distribution
FGS-0639 In distribution
FGS-0583 In distribution
FGS-0591 In distribution
FGS-0626 In distribution
FGS-0510 5 In distribution
FGS-0609 In distribution
FGS-0568 In distribution
FGS-0110 5 In distribution
FGS-0427 In distribution
FGS-0668 5 In distribution
FGS-0667 In distribution
FGS-0674 In distribution
FGS-0501 In distribution
FGS-0665 In distribution
FGS-0662 In distribution
FGS-0612 In distribution
FGS-0497 In distribution
ASM-0355-01 In distribution
FGS-0362 In distribution
FGS-0590 In distribution
FGS-0640 In distribution
FGS-0109 In distribution
FGS-0498 5 In distribution
FGS-0400 10 In distribution
FGS-0391 In distribution
FGS-0389 In distribution
RFB-0355 In distribution
FGS-0325 In distribution
FGS-0613 In distribution
FGS-0707 In distribution
FGS-0585 5 In distribution
FGS-0554 In distribution
RFB-0154 In distribution
FGS-0500 10 In distribution
FGS-0431 In distribution
FGS-0496 In distribution
FGS-0663 10 In distribution
FGS-0661 5 In distribution
FGS-0567 In distribution
FGS-0355 Withdrawn
RFB-0347 Withdrawn
FGS-0180 10 Withdrawn
FGS-0347 Withdrawn
FGS-0279 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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
NaviCam Data Recorder ANX Robotica Corp. 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
K170210 2017-09-01
K170839 2017-05-26
K140284 2014-12-17
K123864 2013-08-12
K103025 2011-05-13
K101250 2011-03-07
K103088 2011-01-14
K101200 2010-09-30
K091405 2009-07-29
K070475 2007-05-07
K062786 2006-10-18
K053639 2006-05-08
K040248 2004-02-17
K032405 2003-10-29
K031033 2003-07-01
K022980 2003-02-27
K022362 2002-08-09
K020341 2002-05-02
DEN010002 2001-08-01

Recalls

The FDA has not published a severity grade for these. 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
2011-03-08 Not classified Device Design The capsule holder can break away from the catheter during endoscopic procedures, necessitating retrieval. 389 2011-12-02
2007-12-13 Not classified Employee error The cards included in the product’s education kit (proposing a clinical algorithm for capsule endoscopy in patients with suspected Crohn’s disease), were printed incorrectly. 1392 units 2010-11-15

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