Balosmark, Inc.
United Statesfrom the FDA registration address FDA FEI 3046434506
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Perfect-O Ostial Positioning Catheter Ref K260289
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3046434506
- DUNS number
- 144849021
- Address
- 2348 Sheffield Dr, Kalamazoo, MI, 49008
Frequently asked questions
How many devices does Balosmark, Inc. have in the registry?
The registry currently lists 2 devices for Balosmark, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Balosmark, Inc.'s devices?
Among its 2 most recently registered devices, Balosmark, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Balosmark, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Balosmark, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Balosmark, Inc. in the registry?
The most recently registered devices listed for Balosmark, Inc. include Perfect-O FA12913 and Perfect-O Ostial Positioning Catheter.