# Spineguard S.A.

- Location (FDA's records): Vincennes, FR
- FDA decisions: 7 (2013–2024): 7 510(k) clearances
- Names in FDA's records: Spineguard S.A. (6); Spineguard (1)
- Product codes: PDQ (5), HBG (1), SCY (1)
- Predicates its devices cite: 9 (6 its own); citations of its devices by later devices: 7 (6 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Spine Vision, Inc.: 2 (https://510kreport.com/company/spine-vision)
- Aurora Spine, Inc.: 1 (https://510kreport.com/company/aurora-spine)

## Firms that cite its devices most
- Waypoint Orthopedics, Inc.: 1 (https://510kreport.com/company/waypoint-orthopedics)

## Its most-cited devices
- K143159: Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2, Cannulated PediGuard Needle 120mm, Cannulated PediGuard Handle; PediGuard Tri Tip Ø4.0mm, PediGuard Tri Tip Ø3.2mm, PediGuard Tri Tip Ø2.5mm, PediGuard Ø2.5mm XS, PediGuard Curv, PediGuard Curv XS (2015), cited by 2
- K152747: DSG Threaded Drill System (2016), cited by 2
- K162884: SpineGuard DSG Zavation Screw System (2017), cited by 1
- K201454: DSG Connect Technology (2021), cited by 1
- K123390: Pediguard Nerve Detector System (2013), cited by 1

## Recent decisions
- K241895: Cannulated PsiFGuard (Sep 26, 2024)
- K220160: PediGuard Threaded (Mar 31, 2022)
- K201454: DSG Connect Technology (Feb 10, 2021)
- K162884: SpineGuard DSG Zavation Screw System (Jan 12, 2017)
- K152747: DSG Threaded Drill System (Jun 10, 2016)
- K143159: Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2, Cannulated PediGuard Needle 120mm, Cannulated PediGuard Handle; PediGuard Tri Tip Ø4.0mm, PediGuard Tri Tip Ø3.2mm, PediGuard Tri Tip Ø2.5mm, PediGuard Ø2.5mm XS, PediGuard Curv, PediGuard Curv XS (Jan 23, 2015)
- K123390: Pediguard Nerve Detector System (Aug 8, 2013)

Source page: https://510kreport.com/company/spineguard