# 3D-Side S.A.

- Location (FDA's records): Mont-Saint-Guibert, BE
- FDA decisions: 4 (2021–2025): 4 510(k) clearances
- Names in FDA's records: 3D-Side S.A. (3); 3D-Side (1)
- Product codes: QIH (2), QHE (1), PBF (1)
- 510(k) review time since 2016: median 103 days, against 134 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 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
- Medacta International S.A.: 1 (https://510kreport.com/company/medacta-international)
- 3D Systems, Inc.: 1 (https://510kreport.com/company/3d-systems)
- Genesis Software Innovations: 1 (https://510kreport.com/company/genesis-software-innovations)

## Firms that cite its devices most
- 3D Lifeprints UK, Ltd.: 1 (https://510kreport.com/company/3d-lifeprints-uk)

## Its most-cited devices
- K212237: 3D-Cut (2021), cited by 1
- K213779: Customize (2022), cited by 1

## Recent decisions
- K243509: Archer PSI System (May 12, 2025)
- K221432: Customize (Aug 3, 2022)
- K213779: Customize (Mar 16, 2022)
- K212237: 3D-Cut (Nov 29, 2021)

Source page: https://510kreport.com/company/3d-side