KSL Biomedical, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3017505309
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3017505309
- Address
- 55 Amherst Villa Road, Buffalo, NY, 14225
Frequently asked questions
How many devices does KSL Biomedical, Inc. have in the registry?
The registry currently lists 1 device for KSL Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list KSL Biomedical, Inc.'s devices?
Among its 1 most recently registered device, KSL Biomedical, Inc. has devices listed in FDA GUDID (1 device).
What risk classes do KSL Biomedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for KSL Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from KSL Biomedical, Inc. in the registry?
The most recently registered devices listed for KSL Biomedical, Inc. include RPR Carbon Antigen 10024-1.