Daniel T Acosta
Country not established
- Devices
- 1
What Daniel T Acosta makes
Daniel T Acosta manufactures custom artificial human eyes, designed for prosthetic or reconstructive applications in ophthalmology. These devices are tailored to individual patient needs, focusing on anatomical accuracy and functional integration with existing structures.
The company’s portfolio is classified under Class I medical devices in the U.S. and is subject to 510(k) clearance through the FDA. The devices are listed under the FDA’s regulatory framework, and the manufacturer operates from the United States.
Catalogue
Custom Artificial Human Eyes Ref K945270
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Daniel T Acosta have in the registry?
The registry currently lists 1 device for Daniel T Acosta. Devices recorded under merged duplicate company entries are counted once.
Which registries list Daniel T Acosta's devices?
Among its 1 most recently registered device, Daniel T Acosta has devices listed in FDA 510(k) (1 device).
What risk classes do Daniel T Acosta's devices fall under?
Among its 1 most recently registered device, the classes recorded for Daniel T Acosta's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Daniel T Acosta in the registry?
The most recently registered devices listed for Daniel T Acosta include CUSTOM ARTIFICIAL HUMAN EYES.