StrykeFlow
Reusable Suction Irrigation Tip, Standard, Non-Vented, Non-Reflective Finish
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.
| 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
| 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
| 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 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
| 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
| 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.
| 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.