Peritec Biosciences, LLC
Country not established
- Devices
- 1
What Peritec Biosciences, LLC makes
Peritec Biosciences, LLC manufactures vascular repair solutions, including polytetrafluoroethylene (PTFE) patches designed for surgical use in repairing blood vessel walls and preventing aneurysms or dissections. These products are intended for off-the-shelf application in procedures requiring durable, biocompatible reinforcement of arterial structures.
The company’s portfolio is regulated under the FDA’s Class II device classification, requiring premarket notification (510(k)) clearance. The products are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Pfa Patch Ref K041736
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peritec Biosciences, LLC have in the registry?
The registry currently lists 1 device for Peritec Biosciences, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peritec Biosciences, LLC's devices?
Among its 1 most recently registered device, Peritec Biosciences, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Peritec Biosciences, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Peritec Biosciences, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peritec Biosciences, LLC in the registry?
The most recently registered devices listed for Peritec Biosciences, LLC include PFA PATCH.