FDA applicant

Mega Meditex, Ltd.

Bombay 400 021, IN1 decision1995–19950 recalls

FDA records 1 decision for Mega Meditex, Ltd. (Bombay 400 021, IN) in 1995: 1 510(k) clearance. All are in product code LYY (Latex Patient Examination Glove). 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, general hospital panel, where it files most

How often FDA has decided Mega Meditex, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mega Meditex, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mega”

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

Mega Medical, Inc. 7 Mega Motion, Inc. 4 Mega Electronics, Ltd. 4 Mega Services 1 Mega Wijaya Sdn. Bhd. 1 Mega-Tech Intl., Inc. 1

Mega Meditex, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mega”