Blustone Synergy, LLC
United StatesFDA applicant, unverified FDA FEI 3014019090
- Devices
- 142
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 142 devicesShowing 1-50 of 142
Company details
- FDA FEI number
- 3014019090
- DUNS number
- 033467608
- Address
- 5520 Ventana Ct, Pueblo, CO, 81005
- [email protected]
- Phone
- 800-232-9108
Frequently asked questions
How many devices does BLUSTONE SYNERGY, LLC have in the registry?
The registry currently lists 142 devices for BLUSTONE SYNERGY, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list BLUSTONE SYNERGY, LLC's devices?
Among its 50 most recently registered devices, BLUSTONE SYNERGY, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do BLUSTONE SYNERGY, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for BLUSTONE SYNERGY, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BLUSTONE SYNERGY, LLC in the registry?
The most recently registered devices listed for BLUSTONE SYNERGY, LLC include Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) 9000-SP08, Blustone Synergy Cervical Rasp 9017-CRL7, Blustone Synergy Cervical Trial (Slate) 9014-CTL6 and Blustone Synergy Cervical Trial (Slate) 9017-CTP06.