B&W Tek, Inc.
Country not established FDA FEI 3003998872
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- 510(k) 510(k)
Company details
- FDA FEI number
- 3003998872
- Address
- 18 Shea Way Suite 103, Newark, DE, 19713
Frequently asked questions
How many devices does B&W Tek, Inc. have in the registry?
The registry currently lists 1 device for B&W Tek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list B&W Tek, Inc.'s devices?
Among its 1 most recently registered device, B&W Tek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do B&W Tek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for B&W Tek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from B&W Tek, Inc. in the registry?
The most recently registered devices listed for B&W Tek, Inc. include BWF-5 MEDICAL LASER SERIES, 810 NM; 930 NM; 980 NM; 1080 NM.