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Sign in to claim this brandRIGHT MFG. CO., LTD.
US
Last updated May 24, 2026
What RIGHT MFG. CO., LTD. makes
Right Mfg. Co., Ltd. manufactures automated ophthalmic refractometers, ophthalmic examination slit lamps, and bench-top keratometers. These devices are designed for use in eye examinations, including measuring refractive error, assessing corneal curvature, and examining the anterior segment of the eye under controlled lighting.
The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Right Mfg. Co., Ltd. manufacture?
Right Mfg. Co., Ltd. specializes in ophthalmic devices used for eye examinations. Their products include automated ophthalmic refractometers (for measuring refractive error), ophthalmic examination slit lamps (for detailed anterior segment analysis), and bench-top keratometers (for assessing corneal curvature). These devices support clinical assessments in optometry and ophthalmology.
Where is Right Mfg. Co., Ltd. based, and how does that affect its regulatory standing?
Right Mfg. Co., Ltd. is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The FDA classifies their products as either Class I or Class II, depending on risk level, and requires compliance with relevant guidelines for market authorization.
Are Right Mfg. Co., Ltd.’s devices listed in any regulatory registries, and why does this matter?
Yes, Right Mfg. Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, helping healthcare providers verify device authenticity, recall status, and compliance with regulatory requirements. Listing in the UDI system is a key step for devices to be legally marketed in the U.S.
How are Right Mfg. Co., Ltd.’s devices classified by the FDA, and what does that classification mean?
Right Mfg. Co., Ltd.’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls (e.g., labeling, manufacturing practices), while Class II devices involve moderate risk and may need additional performance standards or special controls. Classification determines the regulatory pathway and scrutiny required for market authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- rightmfg.co.jp
- —
- —
- [email protected]
- Phone
- +81223593113
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 713383495
Catalogue (69)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Righton | Retinomax 5 | FDA UDI | Class I | Unknown |
| Righton | Retinomax K+Screeen | FDA UDI | Class I | Unknown |
| Righton | Retinomax K-plus5 | FDA UDI | Class I | Unknown |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Righton | ACOMOREF2 K-Model | FDA UDI | Class I | Unknown |
| Visionix | MW50D | FDA UDI | Class II | Active |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Righton | Retinomax K-plus5 | FDA UDI | Class I | Unknown |
| Visionix | Speedy-K2 | FDA UDI | Class I | Active |
| Visionix | Retinomax Screeen | FDA UDI | Class I | Active |
| Righton | Speedy-K2 | FDA UDI | Class I | Unknown |
| Visionix | MW50D | FDA UDI | Class II | Active |
| Righton | Retinomax K-plus5 | FDA UDI | Class I | Unknown |
| Zoom Slit Lamp | RS-1000 | FDA UDI | Class II | Unknown |
| Visionix | MW50D | FDA UDI | Class II | Active |
| Visionix | Retinomax Screeen | FDA UDI | Class I | Active |
| Visionix | Retinomax 5 | FDA UDI | Class I | Active |
| Righton | Retinomax 5 | FDA UDI | Class I | Unknown |
| Visionix | Retinomax Screeen | FDA UDI | Class I | Active |
| Visionix | MW50D | FDA UDI | Class II | Active |
| Visionix | Retinomax K+Screeen | FDA UDI | Class I | Active |
| Righton | Retinomax K+Screeen | FDA UDI | Class I | Unknown |
| Righton | Retinomax Screeen | FDA UDI | Class I | Unknown |
| Righton | Retinomax K-plus5 | FDA UDI | Class I | Unknown |
| Visionix | Retinomax 5 | FDA UDI | Class I | Active |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Righton | Retinomax K+Screeen | FDA UDI | Class I | Unknown |
| Visionix | Retinomax 5 | FDA UDI | Class I | Active |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Zoom Slit Lamp | RS-1000 | FDA UDI | Class II | Unknown |
| Righton | Retinomax Screeen | FDA UDI | Class I | Unknown |
| Righton | Aspherical Lens 14D | FDA UDI | Class I | Unknown |
| Righton | Retinomax K+Screeen | FDA UDI | Class I | Unknown |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Righton | Retinomax 5 | FDA UDI | Class I | Unknown |
| Righton | Retinomax Screeen | FDA UDI | Class I | Unknown |
| Zoom Slit Lamp | NS-2D | FDA UDI | Class II | Unknown |
| Righton | Retinomax 5 | FDA UDI | Class I | Unknown |
| Righton | Aspherical Lens 78D | FDA UDI | Class I | Unknown |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Visionix | Retinomax K+Screeen | FDA UDI | Class I | Active |
| Led Slit Lamp | MW50D | FDA UDI | Class II | Unknown |
| Visionix | Retinomax K-plus5 | FDA UDI | Class I | Active |
| Visionix | Retinomax K-plus5 | FDA UDI | Class I | Active |
| Righton | Retinomax Screeen | FDA UDI | Class I | Unknown |
| Visionix | MW50D | FDA UDI | Class II | Active |
| Righton | Retinomax 5 | FDA UDI | Class I | Unknown |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Right Mfg. Co., Ltd. Itabashi-Ku Tokyo · JP FEI 3004438257