Adcura, Inc.
United Statesfrom the FDA registration address FDA FEI 3013758617
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Adcura, Inc. makes
Adcura, Inc. manufactures lateral lumbar interbody fusion devices designed for spinal stabilization, including the Adcura® Sagittae® system for lateral lumbar interbody fusion procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. Adcura, Inc. is headquartered in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3013758617
- Address
- 18300 Minnetonka Blvd Ste 210, Wayzata, MN, 55391
Frequently asked questions
How many devices does Adcura, Inc. have in the registry?
The registry currently lists 1 device for Adcura, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adcura, Inc.'s devices?
Among its 1 most recently registered device, Adcura, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Adcura, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Adcura, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adcura, Inc. in the registry?
The most recently registered devices listed for Adcura, Inc. include Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices.