FDA applicant
Medtexx Manufacturing Sdn. Bhd.
FDA records 4 decisions for Medtexx Manufacturing Sdn. Bhd. (Kamunting, Taiping, Perak, MY) from 2007 to 2012: 4 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and LZA (Polymer Patient Examination Glove). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Medtexx Manufacturing Sdn. Bhd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2012
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medtexx Manufacturing Sdn. Bhd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Medtexx”
FDA records each applicant name separately; these may or may not be the same firm.