Titmus Optical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Titmus Optical, Inc. makes
Titmus Optical, Inc. manufactures optical testing instruments, including the CRISTY/COTE for visual acuity assessment, the Titmus Vision Tester II for eye alignment and function evaluation, and the Miller/Nadler Glare Tester for measuring visual discomfort under glare conditions.
These devices are regulated under FDA Class I and Class II classifications, with some models authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
Cristy/Cote Ref K843096
Regimes: 510(k) Registry: 510(k)Titmus Vision Tester Ii Ref K844694
Regimes: 510(k) Registry: 510(k)Miller/Nadler Glare Tester Ref K832762
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Titmus Optical, Inc. have in the registry?
The registry currently lists 3 devices for Titmus Optical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Titmus Optical, Inc.'s devices?
Among its 3 most recently registered devices, Titmus Optical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Titmus Optical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Titmus Optical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Titmus Optical, Inc. in the registry?
The most recently registered devices listed for Titmus Optical, Inc. include CRISTY/COTE, TITMUS VISION TESTER II and MILLER/NADLER GLARE TESTER.