Fehling Surgical Instruments, Inc.
Country not established
- Devices
- 1
What Fehling Surgical Instruments, Inc. makes
Fehling Surgical Instruments, Inc. manufactures vascular occlusion devices, including the SUPERPLAST Double-Occluder for temporary or permanent vascular control, and the SUPERPLAST Vascular Probe for intraoperative vascular assessment.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fehling Surgical Instruments, Inc. have in the registry?
The registry currently lists 1 device for Fehling Surgical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fehling Surgical Instruments, Inc.'s devices?
Among its 1 most recently registered device, Fehling Surgical Instruments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fehling Surgical Instruments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fehling Surgical Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fehling Surgical Instruments, Inc. in the registry?
The most recently registered devices listed for Fehling Surgical Instruments, Inc. include SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe.