Clinical review pending. Facts on this page are checked against the sources listed below (regulatory records, manufacturer documents, peer-reviewed research). A named clinician will review it before we call it medically reviewed.
Last updated 28 Sep 2026 · How we review
Last updated 28 Sep 2026 · How we review
Sources
- Regulatory recordFDA 510(k) K173961 — Straumann BLX Implant System (510(k) summary) — U.S. Food and Drug Administration, 2018-06-05. Accessed 28 Sep 2026.
- Regulatory recordFDA 510(k) K140091 — Xpeed AnyRidge Internal Implant System (MegaGen) — U.S. Food and Drug Administration, 2014-12-12. Accessed 28 Sep 2026.