FDA applicant

Cupid Limited

Nashik, IN1 decision2020–20200 recalls

FDA records 1 decision for Cupid Limited (Nashik, IN) in 2020: 1 510(k) clearance. 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 Cupid Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Cupid Limited by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Cupid”

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

Cupid Condom, Ltd. 1

Cupid Limited

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cupid”