Artisential Trocar

The ArtiSential Trocar establishes an access path for endoscopic instruments during minimally invasive surgery. Its assembly includes a main body, cannula and obturator, with an optical…

Registry build 21.09.26

The ArtiSential Trocar establishes an access path for endoscopic instruments during minimally invasive surgery. Its assembly includes a main body, cannula and obturator, with an optical element that allows an endoscope to show tissue layers during insertion.

A funnel guides instruments into the cannula and assists introduction of passive multi-joint surgical instruments. The cannula maintains the passage through the tissue for the selected endoscopic tools.

Listed Item

This device is a sterile, single-use instrument intended to create a passageway for endoscopic instruments and provide access through tissues during minimally invasive surgeries (including abdominal, gynecologic, and thoracic procedures).

Procedures and Supply

The trocar is indicated for general, abdominal, thoracic and gynecologic minimally invasive procedures. It is a prescription surgical instrument supplied sterile and intended for single use.

46manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (15), Jiangsu (13), Zhejiang (7). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GCJ
Manufacturer City Province Registered as Device types
Hangzhou Kangji Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Hangzhou Endo Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 19
Beilun Plastech Inc Ningbo Zhejiang Contract manufacturer 13
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Qingdao O-MEC Medical Technology Co., Ltd. Qingdao Shandong Contract manufacturer 6
Shenzhen Jingxintai Houseware Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
MediConcepts Technology (Shenzhen) Company Limited Shenzhen Guangdong Contract manufacturer 5
Qisda Electronics (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Barco (Suzhou) Healthcare Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 4
Jiangsu Bana Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 4
Comhuge Medical Wire AND Harness Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 2

Showing 12 of 46. All 46 manufacturers in China registered for Laparoscope, General & Plastic Surgery

Record

Regulatory record for Artisential Trocar
Listed by LivsMed Inc., South Korea
FDA product code GCJ
Device type Laparoscope, General & Plastic Surgery
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Manufacturer
510(k) K212500
Record published 2026-04-17

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
Storage Storage environment humidity up to 80 % RH; Storage environment temperature 1 to 30 °C
Packaging Box of 5

Catalogue Numbers

Catalogue numbers for Artisential Trocar
Catalogue number Size Status
AT0810 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Elmed Elmed, Inc. 3,796
Surgical Direct Surgical Direct, Inc. 2,319
Novo Surgical Novo Surgical, Inc. 1,320
Elmed Incorporated Elmed, Inc. 911
Laparoscope, General & Plastic Surgery Karl Storz GmbH & Co. KG 774
Snowden-Pencer Steris Corporation 693
Millennium Avalign Technologies, Inc. 683
Hermann Medizintechnik GmbH Hermann Medizintechnik Gmbh 615
Clickline Karl Storz GmbH & Co. KG 582
V. Mueller Carefusion 2200, Inc. 553
Grasping forceps Sopro-Comeg GmbH 462
Gimmi Gimmi Gmbh 387

Showing 12 of 1,584. All products under Laparoscope, General & Plastic Surgery

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K212500 2021-12-03

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