FDA applicant

Nexus CMF, LLC

Golden3 decisions2001–20260 recalls

FDA records 3 decisions for Nexus CMF, LLC (Golden) from 2001 to 2026: 1 510(k) clearance and 2 original PMA approvals. Most are in product codes MPI (Glenoid Fossa Prosthesis) and LZD (Joint, Temporomandibular, Implant). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Nexus CMF, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2007high 1 (2026) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nexus CMF, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Nexus”

FDA records each applicant name separately; these may or may not be the same firm.

Nexus Spine, LLC 19 Nexus Medical, LLC 16 Nexus Co., Ltd. C/O Yama Trans Co., Ltd. 3 Nexus Health Care Products, Ltd. 1

Nexus CMF, LLC

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nexus”