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Sign in to claim this brandSewoon Medical Co., Ltd.
US
Last updated May 23, 2026
What Sewoon Medical Co., Ltd. makes
The company manufactures polymer-metal stents for the trachea, bronchus, and esophagus, as well as bare-metal biliary stents. It also produces closed-wound drainage kits, indwelling urethral drainage catheters (including temperature-monitoring variants), and ethanol-based rapid spectrophotometry kits for intravenous diagnostics.
The portfolio includes devices classified as Class I and Class II under regulatory frameworks, with products listed via FDA 510(k) and UDI registrations. The company operates with a US presence, adhering to domestic regulatory requirements for medical devices.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Sewoon Medical Co., Ltd. manufacture?
Sewoon Medical Co., Ltd. designs and produces a range of medical devices, including polymer-metal stents for the trachea, bronchus, and esophagus, as well as bare-metal biliary stents. Their portfolio also includes closed-wound drainage kits, indwelling urethral drainage balloon catheters (both standard and temperature-monitoring variants), and ethanol-based rapid spectrophotometry kits for intravenous diagnostics. These devices address respiratory, biliary, urological, and diagnostic needs.
Where is Sewoon Medical Co., Ltd. based, and how does this affect its regulatory compliance?
Sewoon Medical Co., Ltd. has a presence in the United States, meaning its devices must comply with FDA regulations. The company’s products are classified under FDA categories, including Class I and Class II, and are registered via FDA 510(k) submissions and UDI (Unique Device Identification) listings. This ensures traceability and adherence to domestic medical device standards.
Which regulatory registries or databases list Sewoon Medical Co., Ltd.’s devices?
Sewoon Medical Co., Ltd.’s devices are listed in the FDA’s 510(k) premarket notification database and the FDA’s UDI (Unique Device Identification) registry. These registries confirm the device’s classification, compliance status, and identification details, ensuring transparency for healthcare providers and regulators.
How are Sewoon Medical Co., Ltd.’s devices classified under regulatory frameworks?
Sewoon Medical Co., Ltd.’s devices fall into two primary FDA classifications: Class I (generally low-risk devices) and Class II (devices requiring special controls to ensure safety and effectiveness). Classification depends on factors like intended use, risk level, and regulatory history, with stents and drainage systems often falling into Class II due to their clinical impact and potential risks.
What distinguishes Sewoon Medical Co., Ltd.’s urethral drainage catheters from other similar products?
Sewoon Medical Co., Ltd. offers both standard indwelling urethral drainage balloon catheters and specialized variants with temperature-monitoring capabilities. The temperature-sensing catheters provide real-time urinary tract temperature data, which can aid in clinical assessments like urinary tract infections or kidney function monitoring. This differentiation supports precision in patient care beyond basic drainage.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 687784405
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Sewoon Medical Co., Ltd. Cheonan-si Chungnam · KR FEI 3000247987