Bobes S.A.
SpainFDA applicant, unverified
- Devices
- 3
What Bobes S.A. makes
Bobes S.A. manufactures ophthalmic diagnostic equipment, including the BOBES Tonometer for measuring intraocular pressure, the BOBES Slit Lamp for examining the anterior segment of the eye, and the BOBES Lens Set for assessing refractive errors and ocular alignment.
The company’s products are regulated under FDA 510(k) clearance requirements, with devices classified as Class I and Class II. They are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Bobes Tonometer Ref K945446
Regimes: 510(k) Registry: 510(k)Bobes Slit Lamp Ref K945445
Regimes: 510(k) Registry: 510(k)Bobes Lens Set Ref K945443
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bobes S.A. have in the registry?
The registry currently lists 3 devices for Bobes S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bobes S.A.'s devices?
Among its 3 most recently registered devices, Bobes S.A. has devices listed in FDA 510(k) (3 devices).
What risk classes do Bobes S.A.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bobes S.A.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bobes S.A. in the registry?
The most recently registered devices listed for Bobes S.A. include BOBES TONOMETER, BOBES SLIT LAMP and BOBES LENS SET.