M Biopsy Semi-Automatic Disposable Biopsy Needle

Semi-Automatic Disposable Biopsy Needle

Registry build 21.09.26
9manufacturers in China registered for this device type
52catalogue numbers in this listing
2510(k) clearances naming this product 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 M Biopsy Semi-Automatic Disposable Biopsy Needle
Listed by Canyon Medical Inc., China
FDA product code KNW
Device type Instrument, Biopsy
Device class Class 2
Regulation 21 CFR 876.1075
Establishment Manufacturer
510(k) K222865
Record published 2023-05-23
Record revised 2024-01-24 (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, manufacturing date

Catalogue Numbers

Catalogue numbers for M Biopsy Semi-Automatic Disposable Biopsy Needle
Catalogue number Size Status
N50116060 In distribution
N50116130 In distribution
N50118100 In distribution
N50114180 In distribution
NS5011630 In distribution
NS5011610 In distribution
N50120160 In distribution
N50118160 In distribution
N50120250 In distribution
N50116200 In distribution
N50114130 In distribution
NS5011618 In distribution
NS5011820 In distribution
N50114060 In distribution
NS5011430 In distribution
N50120200 In distribution
NS5011616 In distribution
N50118060 In distribution
NS5011818 In distribution
NS5011418 In distribution
NS5011816 In distribution
NS5011613 In distribution
NS5012013 In distribution
NS5012016 In distribution
NS5012025 In distribution
NS5012020 In distribution
N50120100 In distribution
NS5011813 In distribution
NS5011413 In distribution
N50114300 In distribution
NS5011825 In distribution
NS5011810 In distribution
N50118130 In distribution
N50118250 In distribution
N50114100 In distribution
N50114200 In distribution
N50118200 In distribution
NS5011420 In distribution
NS5012018 In distribution
N50116300 In distribution
N50120180 In distribution
N50114160 In distribution
N50116100 In distribution
N50116160 In distribution
NS5011416 In distribution
N50120130 In distribution
N50118180 In distribution
NS5011620 In distribution
NS5011410 In distribution
N50116180 In distribution
NS5012010 In distribution
N50120060 In distribution

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
K233031 2024-01-17
K222865 2023-04-03

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