Eyetech, LLC
Country not established
- Devices
- 2
What Eyetech, LLC makes
Eyetech, LLC manufactures UV-absorbing posterior chamber intraocular lenses, designed for implantation during cataract surgery to replace the eye’s natural lens. The company also produces devices for measuring episcleral venous pressure, a key metric in assessing glaucoma and ocular hypertension.
The company’s portfolio includes Class II and Class III devices, regulated under FDA pathways such as the 510(k) and Premarket Approval (PMA) processes. These products are listed in the FDA’s regulatory databases, and the company is headquartered in the United States.
Catalogue
Episcleral Venous Pressure Ref K843354
510(k) 510(k)- PMA PMA
Frequently asked questions
How many devices does Eyetech, LLC have in the registry?
The registry currently lists 2 devices for Eyetech, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eyetech, LLC's devices?
Among its 2 most recently registered devices, Eyetech, LLC has devices listed in FDA 510(k) (1 device) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Eyetech, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eyetech, LLC's devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Eyetech, LLC in the registry?
The most recently registered devices listed for Eyetech, LLC include EPISCLERAL VENOUS PRESSURE and MODEL 14760 UV ABSORBING POSTERIOR CHAMBER LENSES.