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Sign in to claim this brandMEDIVISION, INC.
US
Last updated May 25, 2026
What MEDIVISION, INC. makes
Medivision, Inc. manufactures reusable rigid optical scopes for endoscopic procedures, including arthroscopes, sinoscopes, cystoscopes, hystercoscopes, and laparoscopes. The company also produces single-use surgical and medical face masks designed for clinical and procedural settings.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based 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 Medivision, Inc. primarily manufacture?
Medivision, Inc. specializes in reusable rigid optical scopes used for endoscopic procedures. These include arthroscopes (for joint visualization), sinoscopes (for sinus examination), cystoscopes (for bladder and urinary tract inspection), hystercoscopes (for uterine cavity assessment), and laparoscopes (for abdominal cavity visualization). Additionally, the company produces single-use surgical and medical face masks for clinical and procedural environments.
Where is Medivision, Inc. based, and how does that affect its regulatory oversight?
Medivision, Inc. is based in the United States, which means its devices are subject to FDA regulations. The FDA classifies these devices as Class II, indicating they pose moderate risk and require special controls to ensure safety and effectiveness. This classification helps guide the regulatory requirements and oversight for these products.
Are Medivision, Inc.’s devices listed in any regulatory registries, and why does this matter?
Yes, Medivision, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers, regulators, and other stakeholders to quickly identify and verify the specific devices in use. Listing in the UDI database is particularly important for tracking recalls, compliance, and post-market surveillance.
How are Medivision, Inc.’s devices classified under FDA regulations, and what does that mean for users?
Medivision, Inc.’s devices are classified as Class II under FDA regulations. This classification means they are considered to have a moderate risk and require special controls beyond general controls to ensure their safety and performance. For users, this classification implies that these devices undergo additional scrutiny during manufacturing, labeling, and post-market surveillance to maintain compliance with FDA requirements.
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
- 942192550
Catalogue (25)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Medivision | MVA2731 | FDA UDI | Class II | Active |
| MediVision | MVA445 | FDA UDI | Class II | Active |
| Medivision | MV470 | FDA UDI | Class II | Active |
| Medivision | MV5500 | FDA UDI | Class II | Active |
| Medivision | MV430 | FDA UDI | Class II | Active |
| MediVision | MVA430 | FDA UDI | Class II | Active |
| Medivision | MV2900 | FDA UDI | Class II | Active |
| Medivision | MVA2732 | FDA UDI | Class II | Active |
| Medivision | MVA470 | FDA UDI | Class II | Active |
| Medivision | MV1030 | FDA UDI | Class II | Active |
| PureDefense Surgical Mask | VQN0185B | FDA UDI | Class II | Active |
| Medivision | MVA430S | FDA UDI | Class II | Active |
| Medivision | MV400 | FDA UDI | Class II | Active |
| Medivisiion | MVA2702 | FDA UDI | Class II | Active |
| Medivision | MVA470S | FDA UDI | Class II | Active |
| MediVision | MVA400 | FDA UDI | Class II | Active |
| Medivision | MV1045 | FDA UDI | Class II | Active |
| Medivision | MV5530 | FDA UDI | Class II | Active |
| Medivision | MVA400S | FDA UDI | Class II | Active |
| Medivision | MV412 | FDA UDI | Class II | Active |
| Medivision | MV1000 | FDA UDI | Class II | Active |
| Medivision | MV5545 | FDA UDI | Class II | Active |
| Medivision | MV2930 | FDA UDI | Class II | Active |
| Medivision | MVA2701 | FDA UDI | Class II | Active |
| PureDefense Surgical Mask | VQN0185W | FDA UDI | Class II | Active |
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