HiLiter

Full Core Coaxial Needle with Tip

Registry build 21.09.26
9manufacturers in China registered for this device type
19catalogue numbers in this listing
5510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Zhejiang (4), Jiangsu (3), Guangdong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KNW
Manufacturer City Province Registered as Device types
Zhejiang Curaway Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Plexus (Xiamen) Co., Ltd., Xiamen Fujian Contract manufacturer 3
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Zhejiang Huanyi Sterilization Technology Co., Ltd. Huzhou Zhejiang Contract manufacturer 25
Jiana Sterilization Technology (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 23
Promisemed Hangzhou Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 21
Carbon (Shenzhen) Medical Device Co., Ltd. Shenzhen Guangdong Manufacturer 6
Canyon Medical Inc. Nanjing Jiangsu Manufacturer 4
Suzhou Leapmed Healthcare Corporation Suzhou Jiangsu Contract manufacturer 3

Record

Regulatory record for HiLiter
Listed by Stryker GmbH, Switzerland
FDA product code KNW
Device type Instrument, Biopsy
Device class Class 2
Regulation 21 CFR 876.1075
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2016-09-23
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Pack of 10
Sizes Needle gauge 13 to 19 G
Distribution end date 2018-01-05

Catalogue Numbers

Catalogue numbers for HiLiter
Catalogue number Size Status
0909715000 Distal Length: 15.0 Centimeter In distribution
0908915000 Distal Length: 15.0 Centimeter Withdrawn
0907309000 Distal Length: 9.0 Centimeter Withdrawn
0907310000 Distal Length: 10.0 Centimeter Withdrawn
0907920000 Needle Gauge 19.0 G Withdrawn
0907909000 Needle Gauge 19.0 G Withdrawn
0906315000 Distal Length: 15.0 Centimeter Withdrawn
0909720000 Needle Gauge 17.0 G Withdrawn
0907710000 Distal Length: 10.0 Centimeter Withdrawn
0909710000 Distal Length: 10.0 Centimeter Withdrawn
0907910000 Distal Length: 10.0 Centimeter Withdrawn
0909610000 Distal Length: 10.0 Centimeter Withdrawn
0907520000 Distal Length: 20.0 Centimeter Withdrawn
0906310000 Distal Length: 10.0 Centimeter Withdrawn
0908515000 Needle Gauge 15.0 G Withdrawn
0907709000 Distal Length: 9.0 Centimeter Withdrawn
0907509000 Distal Length: 9.0 Centimeter Withdrawn
0907720000 Distal Length: 20.0 Centimeter Withdrawn
0908715000 Needle Gauge 17.0 G Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Curaway Zhejiang Curaway Medical Technology Co., Ltd. 910
SureAim Coaxial Biopsy Needle Canyon Medical Inc. 157
CorVocet™ Merit Medical Systems, Inc. 157
SureCore Automatic Disposable Biopsy Needle Canyon Medical Inc. 156
M Biopsy Automatic Disposable Biopsy Needle Canyon Medical Inc. 108
M Biopsy Coaxial Biopsy Needle Canyon Medical Inc. 89
Co-Axial Introducer Needle Argon Medical Devices, Inc. 80
SureCore Semi-automatic Disposable Biopsy Needle Canyon Medical Inc. 76
Invivo Philips DS North America LLC 71
Coaxial needle Möller Medical GmbH 68
Disposable needle for reusable biopsy gun Möller Medical GmbH 62
Remington Medical, Inc. Automatic Cutting Needle (NAC) Remington Medical, Inc. 60

Showing 12 of 692. All products under Instrument, Biopsy

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K180327 2018-02-26
K172558 2017-10-05
K143546 2015-03-19
K141673 2014-09-04
K032943 2003-12-17

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
2015-06-02 Class II Employee error Stryker Instruments is recalling the Stryker SelectCore Variable Throw Biopsy Device due to the potential for for the stylet to eject from the SelectCore device during actuation. 55 units 2015-09-03
2015-04-24 Class II Device Design Potential for the device cannula to overthrow past the intended length. 1,420 Units 2015-10-15

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