# Spinalight, Inc.

- Location (FDA's records): Woodstock, GA
- FDA decisions: 7 (1994–2018): 7 510(k) clearances
- Product codes: LXM (4), INQ (2), JFB (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Neuromechanical Innovations, LLC: 1 (https://510kreport.com/company/neuromechanical-innovations)

## Its most-cited devices
- K001476: Torque Instrument, Model 8500 (2000), cited by 1
- K946258: Model 8000 Atlas C-1 Orthogonal Adjusting Instrument (1995), cited by 1

## Recent decisions
- K172536: Atlas Percussion Adjusting Instrument (Jun 20, 2018)
- K001476: Torque Instrument, Model 8500 (Aug 4, 2000)
- K955540: Hand Held Atlas Instrument (Mar 4, 1996)
- K946258: Model 8000 Atlas C-1 Orthogonal Adjusting Instrument (Nov 20, 1995)
- K945954: Models 4100 and 4300 Multitherapy (Jan 19, 1995)
- K933621: Hilo Table (Jan 7, 1994)
- K933622: Flexion Distraction Table (Jan 7, 1994)

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