Odyssey Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Odyssey Technologies, Inc. makes
Odyssey Technologies, Inc. manufactures universal handpieces for ophthalmic surgery, including the P3 and VISTA models designed for phacoemulsification procedures. These devices are intended for use in cataract removal and other anterior segment surgeries, providing precision tools for surgical applications.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. regulatory requirements. Odyssey Technologies, Inc. is headquartered in the United States.
Catalogue
P3 Universal Phaco Handpiece Ref K972253
Regimes: 510(k) Registry: 510(k)Vista Universal Handpiece Ref K972252
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Odyssey Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Odyssey Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Odyssey Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Odyssey Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Odyssey Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Odyssey Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Odyssey Technologies, Inc. in the registry?
The most recently registered devices listed for Odyssey Technologies, Inc. include P3 UNIVERSAL PHACO HANDPIECE and VISTA UNIVERSAL HANDPIECE.