Electro Fiberoptics Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Electro Fiberoptics Corp. makes
Electro Fiberoptics Corp. manufactures arthroscopes, fiber optic endoscopes, and fiber optic lightsources with carriers. These devices are designed for minimally invasive surgical procedures and diagnostic imaging, utilizing fiber optic technology for illumination and visualization.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Arthroscope Ref K943628
Regimes: 510(k) Registry: 510(k)Fiberoptic Lightsources And Carriers Ref K933145
Regimes: 510(k) Registry: 510(k)Fiber Optic Endoscope Ref K921918
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electro Fiberoptics Corp. have in the registry?
The registry currently lists 3 devices for Electro Fiberoptics Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electro Fiberoptics Corp.'s devices?
Among its 3 most recently registered devices, Electro Fiberoptics Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Electro Fiberoptics Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Electro Fiberoptics Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electro Fiberoptics Corp. in the registry?
The most recently registered devices listed for Electro Fiberoptics Corp. include ARTHROSCOPE, FIBEROPTIC LIGHTSOURCES AND CARRIERS and FIBER OPTIC ENDOSCOPE.