Ritm Okb Zao
RU Last updated 23 Oct 2026
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- Devices
- 2
- Registries
- FDA 510(k)FDA
- FDA recalls
- 0
Catalogue
Scenar, Model 10 Ref K092117
What Ritm Okb Zao makes
Ritm Okb Zao manufactures devices from the SCENAR cutaneous electrode family, including models like SCENAR (SCELAP, ENISAR, IPENS) and the SCENAR Model 10. These devices are designed for electrotherapy applications, delivering controlled electrical impulses through cutaneous electrodes for therapeutic purposes.
The company’s portfolio is regulated under Class II medical devices in the US and is listed in the FDA’s 510(k) registry. The devices are based in the United States.
Frequently asked questions
What types of medical devices does Ritm Okb Zao manufacture?
Ritm Okb Zao specializes in devices from the SCENAR cutaneous electrode family, including models like the SCENAR (SCELAP, ENISAR, IPENS) and the SCENAR Model 10. These devices are designed for electrotherapy, delivering controlled electrical impulses through cutaneous electrodes for therapeutic use.
Where is Ritm Okb Zao based?
Ritm Okb Zao is based in the United States. The company’s headquarters and operations are located within the country, where its devices are developed and regulated.
Which regulatory registries list Ritm Okb Zao’s devices?
Ritm Okb Zao’s devices are listed in the FDA’s 510(k) registry. This registry tracks medical devices that have undergone the 510(k) premarket notification process, which is required for Class II devices in the US.
How are Ritm Okb Zao’s devices classified in the US?
Ritm Okb Zao’s devices fall under Class II classification in the US. This classification is assigned based on the level of risk associated with the device, where Class II devices require special controls in addition to general controls to ensure safety and effectiveness.
Information
- Country
- RU
- Address
- 99, PETROVSKAYA, TAGANROG Rostovskaya Oblast'
- FDA FEI number
- 3007028037