Dt Medtech, LLC
Dt Medtech, LLC holds FDA 510(k) medical device clearance, cleared in 2017, with 2 FDA device recalls on record.
Top product codes for Dt Medtech, LLC
FDA recalls by Dt Medtech, LLC
- Z-0402-2019 — DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305 components are prostheses for a mobile bearing ankle joint.
- Z-0403-2019 — DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4 Part Number: 302114 components are prostheses for a mobile bearing ankle joint.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Dt Medtech, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.