Oculinum, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Oculinum, Inc. makes
Oculinum, Inc. manufactures monopolar needle electrodes and monopolar injection needle electrodes, designed for precise medical procedures. The company also produces the Oculinum Injection Amplifier, a device used to enhance injection-based treatments. These products are intended for specialized applications requiring controlled electrical stimulation or fluid delivery.
The company’s portfolio is classified under FDA Class II devices and is authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry. Oculinum, Inc. is based in the United States.
Catalogue
Monopolar Needle Electrode Ref K900098
Regimes: 510(k) Registry: 510(k)Monopolar Injection Needle Electrode Ref K854793
Regimes: 510(k) Registry: 510(k)Oculinum Injection Amplifier Ref K900279
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oculinum, Inc. have in the registry?
The registry currently lists 3 devices for Oculinum, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oculinum, Inc.'s devices?
Among its 3 most recently registered devices, Oculinum, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Oculinum, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Oculinum, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oculinum, Inc. in the registry?
The most recently registered devices listed for Oculinum, Inc. include MONOPOLAR NEEDLE ELECTRODE, MONOPOLAR INJECTION NEEDLE ELECTRODE and OCULINUM INJECTION AMPLIFIER.