StrykeFlow

Reusable Suction Irrigation Tip, Standard, Non-Vented, Non-Reflective Finish

Registry build 21.09.26
46manufacturers in China registered for this device type
26catalogue numbers in this listing
20510(k) clearances naming this product code

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 StrykeFlow
Listed by Stryker GmbH, Switzerland
FDA product code GCJ
Device type Laparoscope, General & Plastic Surgery
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
510(k) K934094
Record published 2016-09-23
Record revised 2023-01-16 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Pack of 6, pack of 10
Sizes Outer diameter 2 to 10 mm; length 24 to 45 cm
Distribution end date 2023-01-14

Catalogue Numbers

Catalogue numbers for StrykeFlow
Catalogue number Size Status
0250070405 Outer Diameter 10.0 mm In distribution
0250070402 Outer Diameter 5.0 mm In distribution
0250070490 Length 32.0 cm In distribution
0250070492 Length 32.0 cm In distribution
0250070500 In distribution
0250070408 Length 45.0 cm In distribution
0250070411 Length 24.0 cm In distribution
0250070409 Length 32.0 cm In distribution
0250070491 Length 32.0 cm In distribution
0250070404 Length 32.0 cm In distribution
0250070403 Outer Diameter 5.0 mm In distribution
0250070472 Length 32.0 cm In distribution
0250070407 Length 32.0 cm In distribution
0250070419 In distribution
0250070437 Outer Diameter 5.0 mm In distribution
0250070406 Length 32.0 cm In distribution
0250070482 Outer Diameter 5.0 mm Withdrawn
0250070487 Outer Diameter 5.0 mm Withdrawn
0250070485 Length 32.0 cm Withdrawn
0250070489 Length 32.0 cm Withdrawn
0250070486 Outer Diameter 5.0 mm Withdrawn
0250070484 Length 32.0 cm Withdrawn
0250070483 Outer Diameter 5.0 mm Withdrawn
0250070488 Outer Diameter 5.0 mm Withdrawn
0250070471 Outer Diameter 2.0 mm Withdrawn
0250070473 Length 34.0 cm Withdrawn

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
K232157 2023-08-18
K230605 2023-03-31
K230216 2023-02-23
K222130 2022-08-19
K221217 2022-06-17
K214046 2022-05-25
K220895 2022-04-22
K212055 2021-12-16
K212511 2021-11-04
K210088 2021-04-13
K210584 2021-03-18
K202592 2020-10-08
K201434 2020-07-28
K200310 2020-03-06
K192172 2019-09-09
K181258 2018-11-05
K182160 2018-11-05
K930224 1994-06-30
K934094 1994-02-18
K910132 1991-02-21

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of StrykeFlow
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Stryker Endoscopy 510(k) number 2025-06-18 Class II Under Investigation by firm Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.
Stryker Endoscopy 510(k) number 2017-11-17 Class II Under Investigation by firm Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates. 60,753 units total 2024-01-29

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