Reichert Ophthalmic Instruments, Div. Leica, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Reichert Ophthalmic Instruments, Div. Leica, Inc. makes
Reichert Ophthalmic Instruments manufactures diagnostic devices for ophthalmology, including the EYECHEK for automated refraction testing, the XPERT NCT for non-contact tonometry, and the REICHERT CT200 for contact tonometry. These instruments are designed to measure eye pressure and refractive error in clinical settings.
The company’s portfolio includes Class I and Class II devices, with several authorised through the FDA’s 510(k) pathway. Products are listed under U.S. regulatory requirements, and the manufacturer operates from the United States.
Catalogue
Eyechek Ref K964290
Regimes: 510(k) Registry: 510(k)Xpert Nct Ref K941865
Regimes: 510(k) Registry: 510(k)Reichert CT200 Contact Tonometer Ref K000288
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Reichert Ophthalmic Instruments, Div. Leica, Inc. have in the registry?
The registry currently lists 3 devices for Reichert Ophthalmic Instruments, Div. Leica, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reichert Ophthalmic Instruments, Div. Leica, Inc.'s devices?
Among its 3 most recently registered devices, Reichert Ophthalmic Instruments, Div. Leica, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Reichert Ophthalmic Instruments, Div. Leica, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Reichert Ophthalmic Instruments, Div. Leica, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Reichert Ophthalmic Instruments, Div. Leica, Inc. in the registry?
The most recently registered devices listed for Reichert Ophthalmic Instruments, Div. Leica, Inc. include EYECHEK, XPERT NCT and REICHERT CT200 CONTACT TONOMETER.