Xper Technology Procheck Witty Procheck Smart Blood Glucose Test Strips

Catalogue number TD-4335, listed by Taidoc Technology Corporation, Taiwan, under System, Test, Blood Glucose, Over The Counter. 20 manufacturers in China are registered for this product code.

Registry build 21.09.26
20manufacturers in China registered for this device type
1catalogue number
65510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (8), Jiangsu (4), Zhejiang (4). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NBW
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Sanmina Kunshan Jiangsu Contract manufacturer 15
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Flextronics Medical Device Manufacturing (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Yasee Biomedical Inc Qingdao Shandong Contract manufacturer 5
Altek Medical (kunshan) limited Kunshan Free Trade Zone Jiangsu Contract manufacturer 2
Dongguan Kaifa Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Andon Health Co., Ltd. Tianjin Tianjin Contract manufacturer 22
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21

Showing 12 of 20. All 20 manufacturers in China registered for System, Test, Blood Glucose, Over The Counter

Record

Regulatory record for Xper Technology Procheck Witty Procheck Smart Blood Glucose Test Strips
Listed by Taidoc Technology Corporation, Taiwan
FDA product code NBW
Device type System, Test, Blood Glucose, Over The Counter
Device class Class 2
Regulation 21 CFR 862.1345
Establishment Contract manufacturer, Repacker / relabeller, Private-label distributor, Manufacturer
Record published 2025-10-30
Record revised 2026-04-13 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Xper Technology Procheck Witty Procheck Smart Blood Glucose Test Strips
Catalogue number Size Status
TD-4335 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
True Metrix Trividia Health, Inc. 40
Fora Fora Care Inc. 31
True Metrix AIR Trividia Health, Inc. 21
GE Bionime Corporation 21
TRUEtrack Trividia Health, Inc. 17
Medline Medline Industries, Inc. 15
AgaMatrix Agamatrix 15
Tenovi Tenovi Co 13
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 11
Accu-Chek Guide Roche Diagnostics Operations 10
Curaplex Bound Tree Medical, LLC 10
OneTouch Verio Lifescan Europe Gmbh 10

Showing 12 of 476. All products under System, Test, Blood Glucose, Over The Counter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201037 2022-06-16
K190579 2019-06-04
K181588 2018-11-30
K173511 2018-07-12
K162382 2017-04-14
K161738 2016-11-10
K151100 2015-09-29
K143467 2015-05-07
K124040 2013-05-16
K113077 2012-08-03
K111890 2012-02-06
K101926 2011-12-20
K112275 2011-12-15
K112963 2011-11-22
K101631 2011-09-02
K101635 2011-08-31
K111029 2011-07-01
K101509 2011-06-27
K102049 2011-05-27
K110948 2011-05-13
K092875 2010-08-13
K100732 2010-07-09
K100322 2010-06-28
K094005 2010-05-05
K093940 2010-04-23
K091555 2010-03-15
K092902 2010-03-02
K093592 2010-02-25
K093712 2010-02-19
K093635 2010-02-18
K093005 2010-02-05
K093035 2009-12-24
K092099 2009-12-10
K091898 2009-09-18
K090188 2009-07-13
K090404 2009-06-23
K090187 2009-05-12
K090185 2009-04-24
K090536 2009-03-26
K081715 2008-12-17
K082169 2008-12-04
K082618 2008-10-07
K081957 2008-08-05
K080283 2008-06-27
K081144 2008-06-23
K080014 2008-06-09
K080501 2008-04-21
K073494 2008-04-02
K073119 2008-03-03
K072784 2007-12-21
K071493 2007-10-26
K072039 2007-10-03
K072489 2007-09-20
K070941 2007-06-21
K070641 2007-04-09
K070472 2007-03-15
K062800 2007-01-12
K063212 2006-11-22
K062235 2006-09-19
K061181 2006-07-06
K051936 2005-08-08
K051854 2005-08-05
K042795 2005-03-07
K042005 2004-08-27
K041107 2004-06-18

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