Oculo-Plastik Reg'D
CanadaFDA applicant, unverified
- Devices
- 1
What Oculo-Plastik Reg'D makes
Oculo-Plastik Reg’D manufactures the Lee Allen’s Universal Motility Implant, a device designed for ocular motility correction, enabling controlled eye movement adjustments.
The company’s product portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Lee Allen's Universal Motility Implant Ref K873578
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oculo-Plastik Reg'D have in the registry?
The registry currently lists 1 device for Oculo-Plastik Reg'D. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oculo-Plastik Reg'D's devices?
Among its 1 most recently registered device, Oculo-Plastik Reg'D has devices listed in FDA 510(k) (1 device).
What risk classes do Oculo-Plastik Reg'D's devices fall under?
Among its 1 most recently registered device, the classes recorded for Oculo-Plastik Reg'D's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oculo-Plastik Reg'D in the registry?
The most recently registered devices listed for Oculo-Plastik Reg'D include LEE ALLEN'S UNIVERSAL MOTILITY IMPLANT.