AllPoints

AllPoints Dressing Change System with Sliding Post Statlock and BioPatch

Registry build 21.09.26
33manufacturers in China registered for this device type
2catalogue numbers in this listing
4recalls on this code

Who Else Makes It

Concentrated in Zhejiang (13), Jiangsu (5), Shandong (4). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KMK
Manufacturer City Province Registered as Device types
Hubei V-Medical Products Co., Ltd. Xiantao Hubei Contract manufacturer 46
Zhejiang Longterm Medical Technology Co., Ltd. Huzhou Zhejiang Contract manufacturer 26
Henso Medical (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 19
Hubei Junyan Medical Science & Technology Co., Ltd. Huanggang Hubei Contract manufacturer 5
Shandong Shinrise Medical Supplies Co., Ltd. Zibo Shandong Contract manufacturer 5
Shandong Shinemed Technology Co., Ltd. Zibo Shandong Contract manufacturer 2
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Zhejiang Lidesen Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 100
Anji Spenq Industrial Co., Ltd. Huzhou Zhejiang Manufacturer 85
Jcmed Tianjin Import AND Export Co., Ltd. Tianjin Tianjin Manufacturer 51
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
Joykey Industrial (Pinghu) Limited Pinghu Zhejiang Contract manufacturer 43

Showing 12 of 33. All 33 manufacturers in China registered for Device, Intravascular Catheter Securement

Record

Regulatory record for AllPoints
Listed by Bard Access Systems, Inc., United States
FDA product code KMK
Device type Device, Intravascular Catheter Securement
Device class Class 1
Regulation 21 CFR 880.5210
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2017-06-28
Record revised 2025-11-20 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Storage environment temperature 20 to 25 °C
Packaging Case of 10

Catalogue Numbers

Catalogue numbers for AllPoints
Catalogue number Size Status
APDCSSB1 In distribution
APDCSFB1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Centurion Centurion Medical Products Corporation 190
CathGrip Argentum Medical, LLC 120
Statlock Bard Access Systems, Inc. 74
Grip-Lok Tidi Products, LLC 44
3M™ Tegaderm™ 3M Company 33
FlexGRIP Bedal International NV 30
3M™ Tegaderm™ 3M Deutschland GmbH 21
LifeBubble Novonate Inc 15
Clik-FIX Starboard Medical, Inc. 12
DeRoyal Deroyal Industries, Inc. 10
Clik-Fix® B. Braun Medical Inc. 10
Medline Medline Industries, Inc. 9

Showing 12 of 97. All products under Device, Intravascular Catheter Securement

Recalls

4 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
2017-04-25 Class II Process control StatLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip. 4,500 units 2017-08-21
2016-12-09 Class II Process design Bard Access Systems announces a voluntary field action for the StatLock Catheter Stabilization Devices because some single unit pouches have been released without unique product identifiers (product code, lot number, expiration date, etc.). 30,000 units total 2017-05-26
2016-12-09 Class II Process design Bard Access Systems announces a voluntary field action for the StatLock Catheter Stabilization Devices because some single unit pouches have been released without unique product identifiers (product code, lot number, expiration date, etc.). 14,500 units total 2017-05-26
2013-06-10 Class II Packaging BARD Access Systems is recalling lot JUWJF283 of StatLock CV Plus Stabilization Butterfly Devices due to incorrect pad assembly used during manufacture. The absence of the hydrocolloid strip on the bottom may pose an incremental risk includ 3,875 units. 2014-05-21

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