Bechtel Medical, Inc.
United Statesfrom the FDA registration address FDA FEI 3043172326
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Bechtel Medical, Inc. makes
Bechtel Medical, Inc. manufactures the Wound Geni NPWT System, a negative pressure wound therapy (NPWT) device designed to promote wound healing by applying controlled suction to the affected area.
The company’s portfolio is regulated under Class II devices in the United States and includes products listed via the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
Wound Geni NPWT System Ref K254019
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043172326
- Address
- 300 Schell Ln Ste 305, Phoenixville, PA, 19460
Frequently asked questions
How many devices does Bechtel Medical, Inc. have in the registry?
The registry currently lists 1 device for Bechtel Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bechtel Medical, Inc.'s devices?
Among its 1 most recently registered device, Bechtel Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bechtel Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bechtel Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bechtel Medical, Inc. in the registry?
The most recently registered devices listed for Bechtel Medical, Inc. include Wound Geni NPWT System.