Migs KIT 3
Kit contains: (1) GTB17, Alexis Contained Extraction System, 17cm (1) C0R47, 12x100mm Kii Balloon Blunt Tip System (3) CFF03, 5x100mm Kii Fios First Entry, Advanced Fixation (1) EB010,…
Kit contains: (1) GTB17, Alexis Contained Extraction System, 17cm (1) C0R47, 12x100mm Kii Balloon Blunt Tip System (3) CFF03, 5x100mm Kii Fios First Entry, Advanced Fixation (1) EB010, Voyant 5mm Fusion Device, 37cm
Who Else Makes It
Concentrated in Guangdong (24), Zhejiang (13), Shanghai (10). 23 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 77 |
| Shandong Weigao Orthopaedic Device Co., Ltd. | Weihai | Shandong | Contract manufacturer | 42 |
| Hangzhou Kangji Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 27 |
| Modern Medical Equipment Manufacturing Ltd. | Heng Li, Dongguan | Guangdong | Contract manufacturer | 26 |
| Amphenol Alden Products Company | Shenzhen | Guangdong | Contract manufacturer | 24 |
| Hangzhou Endo Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 19 |
| Hong Qiangxing (Shen Zhen) Electronics Limited | Shenzhen | Guangdong | Contract manufacturer | 19 |
| Shenzhen MED-Link Electronics Tech Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 18 |
| Sanbor Medical Xiamen, Inc. | Xiamen | Fujian | Contract manufacturer | 16 |
| ATL Technology DG,Ltd. | Dongguan | Guangdong | Contract manufacturer | 14 |
| Jiangyin Sinbon Electronics Co Ltd | Jiangyin | Jiangsu | Contract manufacturer | 13 |
| Guangzhou Huada Biotechnology Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 9 |
Showing 12 of 65. All 65 manufacturers in China registered for Electrosurgical, Cutting & Coagulation & Accessories
Record
| Listed by | Applied Medical Resources Corp., United States |
|---|---|
| FDA product code | GEI |
| Device type | Electrosurgical, Cutting & Coagulation & Accessories |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4400 |
| Establishment | Contract manufacturer, Complaint-file establishment, Manufacturer |
| Record published | 2018-05-09 |
| Record revised | 2023-04-04 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| GK160 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Surgical Direct | Surgical Direct, Inc. | 5,729 |
| Speedlock | National Advanced Endoscopy Devices, Inc. | 5,212 |
| Stingray Surgical Products | Stingray Surgical Products L.L.C. | 4,647 |
| Kirwan | Kirwan Surgical Products, LLC. | 1,901 |
| Millennium | Avalign Technologies, Inc. | 1,779 |
| DANmed | Dannoritzer Medizintechnik GmbH & Co. KG | 1,590 |
| Elmed | Elmed, Inc. | 1,519 |
| Symmetry Olsen | Aspen Surgical Products, Inc. | 1,219 |
| Guenter Bissinger Medizintechnik GmbH | Günter Bissinger Medizintechnik GmbH | 1,117 |
| Ambler Surgical | Ambler Surgical, LLC | 756 |
| V. Mueller | Steris Corporation | 661 |
| Aesculap | Aesculap AG | 544 |
Showing 12 of 2,922. All products under Electrosurgical, Cutting & Coagulation & Accessories
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K252740 | 2025-11-04 |
| K252412 | 2025-10-31 |
| K222284 | 2022-10-14 |
| K201212 | 2020-06-05 |
| K200598 | 2020-04-08 |
| K193292 | 2019-12-20 |
| K182653 | 2018-11-14 |
| K182244 | 2018-10-11 |
| K180699 | 2018-04-13 |
| K172624 | 2018-02-13 |
| K171684 | 2017-08-07 |
| K162676 | 2016-12-01 |
| K153017 | 2016-07-06 |
| K153288 | 2016-06-01 |
| K151480 | 2016-02-19 |
| K143536 | 2015-04-16 |
| K143517 | 2015-03-27 |
| K141288 | 2014-08-22 |
| K132300 | 2014-01-24 |
| K103282 | 2010-11-16 |
| K925984 | 1993-06-17 |
Recalls
2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2018-12-12 | Class II | Device Design | Unintentional shifting of the tip insulation of the firm’s electrosurgical probes. | 28 units Domestically – 112 units Internationally | 2021-01-22 |
| 2015-07-31 | Class II | Device Design | Potential to improperly characterize tissue within the jaws, which may result in nonoptimal power delivery. | 101 units (U.S) and 38 units (International) | 2015-11-20 |
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.