KMC Working Channel, 10 Gauge

Catalogue number KMC-008-01, listed by Shanghai KiNETIC Medical Co Ltd, China, under Cement, Bone, Vertebroplasty. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1), Zhejiang (1).

Chinese manufacturers registered for FDA product code NDN
Manufacturer City Province Registered as Device types
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai KiNETIC Medical Co Ltd Shanghai Shanghai Contract manufacturer 19
Ningbo Hicren Biotechnology Co., Ltd. Ningbo Zhejiang Manufacturer 5
Jieno Youcheng Medical Technology (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 3
Dragon Crown Medical Co., Ltd. Jinan Shandong Manufacturer 2

Record

Regulatory record for KMC Working Channel, 10 Gauge
Listed by Shanghai KiNETIC Medical Co Ltd, China
FDA product code NDN
Device type Cement, Bone, Vertebroplasty
Device class Class 2
Regulation 21 CFR 888.3027
Establishment Contract manufacturer, Manufacturer
510(k) K113742
Record published 2020-10-01

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
Storage Storage environment humidity up to 80 % RH; Storage environment temperature 18 to 25 °C
Sizes Needle gauge 10 G

Catalogue Numbers

Catalogue numbers for KMC Working Channel, 10 Gauge
Catalogue number Size Status
KMC-008-01 Needle Gauge 10 G In distribution

Same Product Code

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Product Sold by Catalogue numbers
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Tracker Plus Kyphoplasty System GS Medical Co., Ltd. 25
StabiliT MX Fracture Kit Dfine, Inc. 12
Osseoflex® Merit Medical Systems, Inc. 8
Synth™ BES Imedicom Co., Ltd. 8
Tracker GS Medical Co., Ltd. 6
AVAflex Stryker GmbH 6

Showing 12 of 210. All products under Cement, Bone, Vertebroplasty

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K113742 2012-09-17

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