Expanded Optics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Expanded Optics, Inc. makes
Expanded Optics, Inc. manufactures rigid endoscopes, including the OMNI Laparoscope for abdominal procedures, the OMNI Cystoscope for bladder examinations, and the OMNI Arthroscope for joint surgeries. The company also produces a Universal Light Cable designed for compatibility with these scopes.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Omni Laparoscope Ref K922319
510(k) 510(k)Omni Cystoscope Ref K922320
510(k) 510(k)Omni Arthroscope Ref K922321
510(k) 510(k)Universal Light Cable Ref K894570
510(k) 510(k)
Frequently asked questions
How many devices does Expanded Optics, Inc. have in the registry?
The registry currently lists 4 devices for Expanded Optics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Expanded Optics, Inc.'s devices?
Among its 4 most recently registered devices, Expanded Optics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Expanded Optics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Expanded Optics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Expanded Optics, Inc. in the registry?
The most recently registered devices listed for Expanded Optics, Inc. include OMNI LAPAROSCOPE, OMNI CYSTOSCOPE, OMNI ARTHROSCOPE and UNIVERSAL LIGHT CABLE.