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SpineNet LLC

United Statesfrom the FDA registration address FDA establishment FEI 3006755626

Devices
53
Registrations
FDA
FDA recalls
2

Catalogue53

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Company details

FDA FEI number
3006755626
Address
901 N. Lake Destiny Rd, Maitland, FL, 32751

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2013

    • 5 Feb 2013 Z-2103-2013 Class II Terminated The recall decision has been made because because it has recently been determined that the instructions for use (IFU) had certain statements that should have been removed prior to initial product marketing. Distribution: USA Nationwide Distribution in the state of Florida Submission number: K110733
    • 4 Feb 2013 Z-2107-2013 Class II Terminated SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval. Distribution: Distributed to one customer in Florida.

This is an FDA establishment record. No EUDAMED registration is known for this company.