Fibertech Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Fibertech Instruments, Inc. makes
Fibertech Instruments, Inc. manufactures a button lubricator, a device used to apply lubrication to endoscopic instruments, and the ScopeJockey, a tool designed to assist in the handling and positioning of endoscopes during procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Button Lubricator Ref K951713
Regimes: 510(k) Registry: 510(k)Scopejockey Ref K940780
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fibertech Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Fibertech Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fibertech Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Fibertech Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Fibertech Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fibertech Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fibertech Instruments, Inc. in the registry?
The most recently registered devices listed for Fibertech Instruments, Inc. include BUTTON LUBRICATOR and SCOPEJOCKEY.