FDA applicant

Nexmed, Inc.

Palm Desert, CA6 decisions1995–20040 recalls

FDA records 6 decisions for Nexmed, Inc. (Palm Desert, CA) from 1995 to 2004: 6 510(k) clearances. Most are in product codes LPH (Prosthesis, Hip, Semi-Constrained…) and JDG (Prosthesis, Hip, Femoral Component, Cemented…). 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, orthopedic panel, where it files most

How often FDA has decided Nexmed, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nexmed, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Nexmed”

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

Nexmed Technology Co., Ltd. 1

Nexmed, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Nexmed”