Imedicom Co., Ltd.
16 product lines across 1 device categories: Kyphoplasty systems.
From imedicom.co.kr, checked November 2026.
About Imedicom Co., Ltd.
Imedicom Co., Ltd. hasn't added a company description yet.
Vertebral Augmentation Systems (Kyphoplasty and Vertebroplasty)
Used in: Kyphoplasty, Vertebroplasty
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| MEDINAUT Plus Kyphoplasty System | β | 114 | Not stated |
| Synth Plus | β | 63 | Not stated |
| Synth Plus Bilateral | β | 48 | Not stated |
| SteriSpine VA MEDINAUT Plus | β | 16 | Not stated |
| Synth Bes NOT USE | β | 8 | Not stated |
| Synth Cds | β | 7 | Not stated |
| MEDINAUT-X(IBE System) | β | 7 | Not stated |
| Synth Standard | β | 6 | Not stated |
| MEDINAUT Kyphoplasty System | β | 6 | Not stated |
| MEDINAUT-I(ICD System) | β | 6 | Not stated |
| B-Two Vertebral Balloon Expand Kyphoplasty System | β | 3 | Not stated |
| B-Two Inflatable bone expander system balloon catheter | β | 3 | Not stated |
| Mvx US | β | 1 | Not stated |
| B-Two Inflatable bone expander system syringe | β | 1 | Not stated |
| B-Two Vertebral access system | β | 1 | Not stated |
| MVX Plus | β | 1 | Not stated |
Sales representatives
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From imedicom.co.kr, checked November 2026.
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Frequently asked questions
What devices does Imedicom Co., Ltd. make?
Imedicom Co., Ltd. has 16 product lines in our library across 1 device category: Kyphoplasty systems.
How do I contact a Imedicom Co., Ltd. sales representative?
Imedicom Co., Ltd. has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.
Does LA Vascular sell Imedicom Co., Ltd. products?
No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Imedicom Co., Ltd. or its representatives to buy.
Where do the Imedicom Co., Ltd. product sizes come from?
From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.
Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.