FDA applicant
Cranberry (M) Sdn. Bhd.
FDA records 4 decisions for Cranberry (M) Sdn. Bhd. (Ipoh Perak, MY) from 1989 to 1999: 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 Cranberry (M) Sdn. Bhd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cranberry (M) Sdn. Bhd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cranberry (M) 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) Report