Schott Fiber Optics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Schott Fiber Optics, Inc. makes
Schott Fiber Optics, Inc. manufactures flexible immersible sigmoidoscopes and hysteroscopes, designed for endoscopic procedures in the gastrointestinal and gynecological tracts. These devices are intended for visual inspection and diagnostic purposes within the colon and uterus, respectively.
The company’s portfolio is regulated under Class II medical devices in the United States, with products listed via the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
Flexible Immersible Sigmoidoscope Ref K892000
Regimes: 510(k) Registry: 510(k)Flexible Immersible Hysteroscope Ref K892390
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schott Fiber Optics, Inc. have in the registry?
The registry currently lists 2 devices for Schott Fiber Optics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schott Fiber Optics, Inc.'s devices?
Among its 2 most recently registered devices, Schott Fiber Optics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Schott Fiber Optics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Schott Fiber Optics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schott Fiber Optics, Inc. in the registry?
The most recently registered devices listed for Schott Fiber Optics, Inc. include FLEXIBLE IMMERSIBLE SIGMOIDOSCOPE and FLEXIBLE IMMERSIBLE HYSTEROSCOPE.