# Aptis Medical, LLC

- Location (FDA's records): Glenview, KY
- FDA decisions: 5 (2005–2019): 5 510(k) clearances
- Product codes: KXE (5)
- Predicates its devices cite: 6 (6 its own); citations of its devices by later devices: 6 (6 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K082839: Distal Radio-Ulnar Joint Implant (2008), cited by 2
- K040497: Distal Radio-Ulnar Joint Implant (2005), cited by 2
- K142569: Aptis Medical Distal Radio Ulnar Joint Implant (2015), cited by 1
- K053119: Distal Radio-Ulnar Joint Implant (2005), cited by 1

## Recent decisions
- K190599: Aptis Medical Distal Radio Ulnar Joint Implant (May 3, 2019)
- K142569: Aptis Medical Distal Radio Ulnar Joint Implant (Apr 3, 2015)
- K082839: Distal Radio-Ulnar Joint Implant (Oct 24, 2008)
- K053119: Distal Radio-Ulnar Joint Implant (Dec 7, 2005)
- K040497: Distal Radio-Ulnar Joint Implant (Jan 26, 2005)

Source page: https://510kreport.com/company/aptis-medical