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Aurora Spine, Inc.

Also registered as Aurora Spine

United StatesFDA applicant, unverified FDA FEI 3010326971

Aurora Spine, Inc. is a medical device manufacturer, with 2,919 devices listed in FDA GUDID and FDA 510(k) (FDA Class II, Class I and Unclassified) as of 12 Nov 2026.

Devices
2,919
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 2,909
  • FDA 510(k) 10

A device listed in two registries counts in both.

Device classes
  • FDA Class II 2,677
  • FDA Class I 241
  • FDA Unclassified 1
Identifiers
  • FDA FEI 3010326971
  • DUNS 079119091

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Aurora Spine, Inc. makes

AURORA SPINE, INC. manufactures polymeric and metallic spinal fusion cages, orthopaedic surgical procedure kits, internal orthopaedic fixation systems, spinal fixation plates, instrument trays, sacroiliac joint transarticular fixation/arthrodesis implantation kits, and sterilization packaging.

The company's products are listed in the FDA UDI registry and include Class I and Class II devices.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2,919

Newest first, rows 1-50 of 2,919

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Rows 1-50 of 2,919

Showing 1-50 of 2,919

Company details

FDA FEI number
3010326971
DUNS number
079119091
Address
1930 Palomar Point Way, Carlsbad, CA, 92008
Phone
760.424.2004

Frequently asked questions

How many devices does AURORA SPINE, INC. have in the registry?

The registry currently lists 2919 devices for AURORA SPINE, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list AURORA SPINE, INC.'s devices?

Among its 50 most recently registered devices, AURORA SPINE, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do AURORA SPINE, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for AURORA SPINE, INC.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from AURORA SPINE, INC. in the registry?

The most recently registered devices listed for AURORA SPINE, INC. include Aurora Spine 118-600-01-02, Aurora Spine 118-600-02-01, Aurora Spine 119-302-3038 and Aurora Spine 118-600-02-02.

Generated automatically from registry data and not verified by a human reviewer.