Spinal Simplicity, LLC
United StatesFDA applicant, unverified FDA FEI 3009704301
Spinal Simplicity, LLC is a medical device manufacturer, with 208 devices listed in FDA GUDID and FDA 510(k) (FDA Class I and II) as of 13 Nov 2026.
- Devices
- 208
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 191
- FDA 510(k) 17
- Device classes
- FDA Class I 140
- FDA Class II 68
- Identifiers
- FDA FEI 3009704301
- DUNS 963359513
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 208 devicesShowing 1-50 of 208
Company details
- FDA FEI number
- 3009704301
- DUNS number
- 963359513
- Address
- 6363 College Blvd, Overland Park, KS, 66211
- Website
- www.spinalsimplicity.com
- facebook.com/spinalsimplicity
- Phone
- 913-451-4414
From the company website
Spinal Simplicity is a medical device company dedicated to creating simple, innovative procedure solutions for our physician partners to help improve their patient’s pain and quality of life.
Frequently asked questions
How many devices does Spinal Simplicity, LLC have in the registry?
The registry currently lists 208 devices for Spinal Simplicity, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinal Simplicity, LLC's devices?
Among its 50 most recently registered devices, Spinal Simplicity, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Spinal Simplicity, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Spinal Simplicity, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinal Simplicity, LLC in the registry?
The most recently registered devices listed for Spinal Simplicity, LLC include Minuteman 10-0220-000, Minuteman 10-0221-000, Minuteman 10-0222-000 and Minuteman 10-0223-000.