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US
Last updated May 27, 2026
What OCUMETRICS INC makes
Ocumetrics Inc manufactures the Fluorotron Master, a diagnostic ophthalmic slit lamp designed for retinal imaging and fluorescein angiography to assess retinal vascular conditions and detect abnormalities.
The Fluorotron Master is classified as a Class II medical device and is 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 Ocumetrics Inc manufacture?
Ocumetrics Inc specializes in ophthalmic diagnostic devices. Their primary product is the Fluorotron Master, which is a slit lamp designed specifically for retinal imaging and fluorescein angiography. This device helps clinicians assess retinal vascular conditions and identify abnormalities during eye examinations.
Where is Ocumetrics Inc based?
Ocumetrics Inc is headquartered in the United States. The company’s location is relevant for understanding its regulatory and operational context, particularly in relation to FDA compliance and market distribution.
How are Ocumetrics Inc’s devices classified under medical device regulations?
The Fluorotron Master, the main device produced by Ocumetrics Inc, is classified as a Class II medical device. This classification is determined by the FDA based on factors like the device’s intended use and potential risk to patients, requiring specific regulatory controls to ensure safety and effectiveness.
Are Ocumetrics Inc’s devices listed in any regulatory registries?
Yes, the Fluorotron Master is included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the U.S. market, ensuring transparency and traceability for healthcare providers and regulators.
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
- 807960844
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fluorotron Master | FM-Win | FDA UDI | Class II | Unknown |
| Fluorotron Master | FM-Win | FDA UDI | Class II | Active |
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