The Lebanon Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What The Lebanon Corp. makes
The Lebanon Corp. manufactures ophthalmic diagnostic tools, including the Lebanon Microscope for eye examinations and the Relief Valve for intraocular pressure regulation. It also produces the Ocular Pressure Applicator, a device used in measuring eye pressure during clinical assessments.
The company’s portfolio includes Class I and Class II devices, with some products listed under the FDA’s 510(k) pathway. These devices are regulated under US medical device laws and are based in the United States.
Catalogue
Lebanon Microscope Ref K821689
Regimes: 510(k) Registry: 510(k)Relief Valve-Honan Intraoc. Pressure Ref K820526
Regimes: 510(k) Registry: 510(k)Ocular Pressure Applicator Ref K841652
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Lebanon Corp. have in the registry?
The registry currently lists 3 devices for The Lebanon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Lebanon Corp.'s devices?
Among its 3 most recently registered devices, The Lebanon Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do The Lebanon Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for The Lebanon Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Lebanon Corp. in the registry?
The most recently registered devices listed for The Lebanon Corp. include LEBANON MICROSCOPE, RELIEF VALVE-HONAN INTRAOC. PRESSURE and OCULAR PRESSURE APPLICATOR.