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Sign in to claim this brandScivita Medical Technology Co., Ltd.
US
Last updated May 30, 2026
What Scivita Medical Technology Co., Ltd. makes
Scivita Medical Technology Co., Ltd. manufactures single-use medical devices for endoscopic procedures, including urinary stone retrieval baskets for fragment extraction, flexible endoscopic biopsy forceps for tissue sampling, and single-use flexible video bronchoscopes for airway visualization. The company also produces general specimen containers designed for in vitro diagnostics without additives or media.
The portfolio includes devices classified as Class I and Class II under FDA regulations, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The company is headquartered in the United States.
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 Scivita Medical Technology Co., Ltd. manufacture?
Scivita Medical Technology Co., Ltd. specializes in single-use medical devices primarily used in endoscopic procedures. Their portfolio includes urinary stone retrieval baskets for removing fragments during lithotripsy, flexible endoscopic biopsy forceps for obtaining tissue samples, and single-use flexible video bronchoscopes for visualizing airways. They also produce general specimen containers intended for in vitro diagnostics without additives or media.
Where is Scivita Medical Technology Co., Ltd. based?
The company is headquartered in the United States. This location is relevant for regulatory oversight and compliance, as it aligns with the jurisdiction of the FDA’s regulatory framework.
Which regulatory registries list Scivita Medical Technology Co., Ltd.’s devices?
Scivita Medical Technology Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, allowing them to verify device details and compliance information.
How are Scivita Medical Technology Co., Ltd.’s devices classified under FDA regulations?
Scivita Medical Technology Co., Ltd.’s devices fall into two primary classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and scrutiny each device undergoes.
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
- 544519831
Catalogue (38)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Single-use Biopsy Forceps | BFUW-2311 | FDA UDI | Class I | Unknown |
| Sample Container | SC-60 | FDA UDI | Class I | Active |
| Single-use Broncho Videoscope | SBV-1B-B | FDA UDI | Class II | Unknown |
| Single-use Biopsy Forceps | BFTW-1829E-YG | FDA UDI | Class I | Active |
| Single-use Biopsy Forceps | BFUN-1829E-YG | FDA UDI | Class I | Active |
| Single-use Extraction Baskets | EBF-1529SG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-1508SG | FDA UDI | Class II | Active |
| Single-use Broncho Videoscope | SBV-1A-B | FDA UDI | Class II | Active |
| Single-use Biopsy Forceps | BFUW-1811 | FDA UDI | Class I | Active |
| Single-use Extraction Baskets | EBF-2006SG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-2029SG | FDA UDI | Class II | Active |
| Single-use Broncho Videoscope | SBV-1A-P | FDA UDI | Class II | Unknown |
| Single-use Broncho Videoscope | SBV-1C-B | FDA UDI | Class II | Unknown |
| Single-use Extraction Baskets | EBF-1511SG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-2029CG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-1508CG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-2008SG | FDA UDI | Class II | Active |
| Single-use Broncho Videoscope | SBV-1C-P | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-1506CG | FDA UDI | Class II | Active |
| Single-use Biopsy Forceps | BFUW-1829E-YG | FDA UDI | Class I | Active |
| Single-use Extraction Baskets | EBF-2007CG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-1506SG | FDA UDI | Class II | Active |
| Single-use Biopsy Forceps | BFUW-1629E-YG | FDA UDI | Class I | Active |
| Bronchus Sampler | BS-6060 | FDA UDI | Class I | Active |
| Single-use Biopsy Forceps | BFTN-2311 | FDA UDI | Class I | Unknown |
| Single-use Extraction Baskets | EBF-2008CG | FDA UDI | Class II | Active |
| Single-use Biopsy Forceps | BFTN-1829E-YG | FDA UDI | Class I | Active |
| Single-use Biopsy Forceps | BFTW-1629E-YG | FDA UDI | Class I | Active |
| Single-use Extraction Baskets | EBF-1507CG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-1529CG | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-1507SG | FDA UDI | Class II | Active |
| Single-use Biopsy Forceps | BFTN-1811 | FDA UDI | Class I | Active |
| Single-use Biopsy Forceps | BFUW-1029P-YG | FDA UDI | Class I | Active |
| Single-use Extraction Baskets | EBF-2006CG | FDA UDI | Class II | Active |
| Single-use Broncho Videoscope | SBV-1B-P | FDA UDI | Class II | Unknown |
| Single-use Extraction Baskets | EBF-1511CG | FDA UDI | Class II | Active |
| Single-use Broncho Videoscope | SBV-1C-P | FDA UDI | Class II | Active |
| Single-use Extraction Baskets | EBF-2007SG | FDA UDI | Class II | Active |
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