FDA applicant

Remed Pharma

Crofton, MD9 decisions2000–20000 recalls

FDA records 9 decisions for Remed Pharma (Crofton, MD) in 2000: 9 510(k) clearances. All are in product code HIS (Condom). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Remed Pharma since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Remed”

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

Remed Co., Ltd. 3

Remed Pharma

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 “Remed”