Data / Medical devices / United States / Spine Innovation, LLC

Spine Innovation, LLC: FDA-registered device maker in Coronado, CA, United States, 1 510(k) clearance

Spine Innovation, LLC is registered with the FDA (registration 3013393446) in Coronado, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 8, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3013393446

Address

1330 Orange Ave Ste 328, Coronado, CA, United States, 92118

Owner or operator

Spine Innovation, LLC (10053371)

Roles

Complaint file establishment, Specification developer

First device listed

July 24, 2026

Registered through

2026

Brand names listed

LOGIC

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

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Updated January 8, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.