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Sign in to claim this brandWhat Wingderm Electro-Optics Ltd. makes
Wingderm Electro-Optics Ltd. manufactures dermatological diode laser systems and thermo-mechanical skin surface treatment systems. Their product examples include the Lasermach PRO, Lasermach PRO Handpiece, and Renuva 1550 devices.
These devices are classified as Class II medical devices and are listed in the FDA UDI registry. 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 does Wingderm Electro-Optics Ltd. make?
Wingderm Electro-Optics Ltd. manufactures dermatological diode laser systems and thermo-mechanical skin surface treatment systems, as stated in the provided device data. Examples of their products include the Lasermach PRO, Lasermach PRO Handpiece, and Renuva 1550 devices. These are the specific product types described in the summary and device categories, and no other products or functions are mentioned in the data.
Where is Wingderm Electro-Optics Ltd. based?
Wingderm Electro-Optics Ltd. is based in the United States, as explicitly stated in the COMPANY and COUNTRY fields of the device data. The summary also confirms the company's location in the United States. No other geographic details about facilities, headquarters, or operational sites are provided in the data.
Which registries list Wingderm Electro-Optics Ltd.'s devices?
Wingderm Electro-Optics Ltd.'s devices are listed in the FDA UDI registry, as indicated in the LISTED IN field of the device data. This is the only registry mentioned in the provided information. The data does not reference any other national, international, or regional device registries where their products may be listed.
How are Wingderm Electro-Optics Ltd.'s devices classified?
Wingderm Electro-Optics Ltd.'s devices are classified as Class II medical devices, as specified in the DEVICE CLASSES field of the device data. This classification applies to the dermatological diode laser systems and thermo-mechanical skin surface treatment systems they manufacture, including the example devices like Lasermach PRO and Renuva 1550. The data does not assign any other classification to their devices.
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
- —
- DUNS Number
- 554510960
Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Lasermach | WLA-01 | FDA UDI | Class II | Unknown |
| Lasermach PRO | WLA-01 | FDA UDI | Class II | Active |
| Lasermach PRO Handpiece | WLA-01 | FDA UDI | Class II | Active |
| Lasermach PRO Handpiece | WLA-01 | FDA UDI | Class II | Unknown |
| Renuva 1550 | WFB-01 | FDA UDI | Class II | Active |
| Lasermach PRO Handpiece | WLA-01 | FDA UDI | Class II | Active |
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