Home › Device types › NTG
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA product code NTG · Class 3 · Unknown
247
Registered devices
1,692
Adverse events
4
Recalls
0
510(k) clearances
Devices with this code
Hintermann Series H3 — Dt Medtech, LLCSTAR — Stryker GmbHSTAR — Stryker GmbHSTAR PSI Tibia Cut Guide — Trilliant Surgical, LLCSTAR — Stryker GmbHHintermann Series H3 — Dt Medtech, LLCSTAR™ — Stryker GmbHSTAR — Stryker GmbHSTAR™ — Stryker GmbHHintermann Series H3 — Dt Medtech, LLCSTAR — Stryker GmbHHintermann Series H3 — Dt Medtech, LLCSTAR — Stryker GmbH6mm STAR E+ Sliding Core STAR Total Ankle — Trilliant Surgical, LLCSTAR — Stryker GmbHSTAR — Stryker GmbHSTAR — Stryker GmbHHintermann Series H3 — Dt Medtech, LLCSTAR™ — Stryker GmbHSTAR — Stryker GmbHHintermann Series H3 — Dt Medtech, LLCSTAR — Stryker GmbHSTAR — Stryker GmbHHintermann Series H3 — Dt Medtech, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-24 | DT MedTech, LLC | Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant devi |
| 2023-11-21 | Exactech, Inc. | Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag. |
| 2018-09-25 | DT MedTech, LLC | Incorrect package labeling identifying the device |
| 2018-09-25 | DT MedTech, LLC | Incorrect package labeling identifying the device |
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