HK Klein Infiltration Pump+

HK Klein Infiltration Pump+ (KIP-II+)

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Guangdong (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FRN
Manufacturer City Province Registered as Device types
Sanmina Kunshan Jiangsu Contract manufacturer 15
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
JDI Electronics Factory Dongguan Guangdong Contract manufacturer 7
Zyno Electric & Machinery Ltd, Shanghai Shanghai Shanghai Contract manufacturer 1
Sterigenics Shanghai E Beam Ltd. Shanghai Shanghai Contract manufacturer 14

Record

Regulatory record for HK Klein Infiltration Pump+
Listed by HK Surgical, Inc., United States
FDA product code FRN
Device type Pump, Infusion
Device class Class 2
Regulation 21 CFR 880.5725
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2025-09-29

Specifications

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

Catalogue Numbers

Catalogue numbers for HK Klein Infiltration Pump+
Catalogue number Size Status
KIP-II+ In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Port Access Infusion SET Sb-Kawasumi Laboratories, Inc. 76
Cadd ICU Medical, Inc 56
Flow Control Tubing GO Medical Industries PTY. Ltd. 39
Curlin Administration Set Zevex, Inc. 30
ambIT Summit Medical Products, Inc. 27
Beeline motIV Rex Pj Tech LLC 24
RMS Precision Flow Rate TubingTM Repro-Med Systems, Inc. 24
Medfusion ICU Medical, Inc 24
Volumat™ Line Fresenius Kabi AB 24
Outlook® B. Braun Medical Inc. 21
Alaris CareFusion 303, Inc 19
Alpha Source Battery Alpha Source Inc. 17

Showing 12 of 191. All products under Pump, Infusion

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K123822 2013-09-27
K031432 2003-08-07

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