Halifax Biomedical, Inc.
Country not established FDA
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Halifax Biomedical, Inc. makes
Halifax Biomedical, Inc. produces medical devices including the SR SUITE 1.0, HALIFAX BIOMEDICAL TANATLUM BEAD SET, TANTALUM BEAD SET MODEL P003175, MODEL-BASED RSA SOFTWARE, and Halifax Imaging Kit.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. Halifax Biomedical is based in the US.
Catalogue
Sr Suite 1.0 Ref K121345
510(k) 510(k)Halifax Biomedical Tanatlum Bead Set Ref K103417
510(k) 510(k)Tantalum Bead Set, Model P003175 Ref K090581
510(k) 510(k)Model-Based Rsa Software Ref K133966
510(k) 510(k)Halifax Imaging Kit Ref K182880
510(k) 510(k)
FDA establishments
- Halifax Biomedical Inc. Mabou Nova Scotia · CA FEI 3007305589
Frequently asked questions
How many devices does Halifax Biomedical, Inc. have in the registry?
The registry currently lists 5 devices for Halifax Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Halifax Biomedical, Inc.'s devices?
Among its 5 most recently registered devices, Halifax Biomedical, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Halifax Biomedical, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Halifax Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Halifax Biomedical, Inc. in the registry?
The most recently registered devices listed for Halifax Biomedical, Inc. include SR SUITE 1.0, HALIFAX BIOMEDICAL TANATLUM BEAD SET, TANTALUM BEAD SET, MODEL P003175 and MODEL-BASED RSA SOFTWARE.
Which FDA establishments are linked to Halifax Biomedical, Inc.?
1 FDA establishment is linked to Halifax Biomedical, Inc. in the registry; they are listed on the company page.