# Dt Medtech, LLC

- Location (FDA's records): Towson, MD
- FDA decisions: 2 (2017–2019): 1 510(k) clearance and 1 original PMA approval
- Product codes: HSN (1), NTG (1)
- Predicates its devices cite: 10 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Tornier, Inc.: 4 (https://510kreport.com/company/tornier)
- Wrightmedicaltechnologyinc: 3 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Ascension Orthopedics, Inc.: 1 (https://510kreport.com/company/ascension-orthopedics)
- Topez Orthopedics, Inc.: 1 (https://510kreport.com/company/topez-orthopedics)
- Exactech, Inc.: 1 (https://510kreport.com/company/exactech)

## Firms that cite its devices most
- Vilex, LLC: 2 (https://510kreport.com/company/vilex)

## Its most-cited devices
- K171004: Hintermann Series H2 Total Ankle System (2017), cited by 2

## Recent decisions
- P160036: Hintermann Series H3 Total Ankle Replacement System (Jun 4, 2019)
- K171004: Hintermann Series H2 Total Ankle System (Nov 7, 2017)

Source page: https://510kreport.com/company/dt-medtech