# Slk Ortho, LLC

- Location (FDA's records): Long Grove, IL
- FDA decisions: 1 (2023–2023): 1 510(k) clearance
- Product codes: NDN (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 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
- Hyprevention Sas: 1 (https://510kreport.com/company/hyprevention)

## Recent decisions
- K221697: Injection Pin (Kip (02031-02061) (03031-03061)) (Mar 3, 2023)

Source page: https://510kreport.com/company/slk-ortho