Vilex, LLC
Vilex, LLC holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2026.
Top product codes for Vilex, LLC
Recent clearances by Vilex, LLC
- K260900 — DYNEX® External Fixation Systems
- K250304 — TITANEX Screw Systems
- K240475 — Hintermann Series H2 Total Ankle System
- K243408 — TACTIX Vector Syndesmosis System
- K233816 — REDEMPTION Charcot Plating System
- K240035 — TACTIX Vector Syndesmosis System
- K231343 — Redemption Duo Hindfoot Nail System
- K231504 — TITANEX MICROBEAM Screw System, TITANEX ARTEMIS Screw System
- K231493 — NITINEX Memory Compression Staple
- K230462 — OPTIX H2 Patient Specific Instrument System
- K230204 — ALPHALOK Plating System
- K221342 — REDEMPTION Beaming System
- K221558 — ALPHALOK Plating System
- K212348 — ALPHALOK Plating System
- K212552 — Correx Software
- K202143 — Dynex Micro
- K202054 — Dynex Ring Fixation System, Diametrix Ring Fixation System
Data sourced from openFDA. This site is unofficial and independent of the FDA.