FORTISSIMO SPINE

FDA Device Registration & Listing · Knoxville, TN, US · Registration 3037007952

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3037007952
FEI Number
3037007952
Entity Name
FORTISSIMO SPINE
City/State/Country
Knoxville, TN, US
Establishment Address
7205 Lawford Rd, Knoxville, TN 37919, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Fortissimo Spine (Owner Number: 10093024)
Owner / Operator Contact Address
7205 Lawford Rd, Knoxville, TN 37919, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Injection Pin Driver

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HXX Screwdriver Orthopedic Class 1 888.4540 2026-01-16

Official Correspondent

Andrew Dickson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fortissimo Spine
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3037007952. Last updated year: 2026. Please use registration number 3037007952 when referencing this establishment in official correspondence.
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