Syn-Optics
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- Devices
- 1
What Syn-Optics makes
Syn-Optics manufactures the SYN-OPTICS #5200, a medical device designed for ophthalmic applications, specifically for use in refractive surgery procedures.
The SYN-OPTICS #5200 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Syn-Optics #5200 Ref K820624
510(k) 510(k)
Frequently asked questions
How many devices does Syn-Optics have in the registry?
The registry currently lists 1 device for Syn-Optics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syn-Optics's devices?
Among its 1 most recently registered device, Syn-Optics has devices listed in FDA 510(k) (1 device).
What risk classes do Syn-Optics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Syn-Optics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Syn-Optics in the registry?
The most recently registered devices listed for Syn-Optics include SYN-OPTICS #5200.