FDA applicant
Lamberts Dalston, Ltd.
FDA records 1 decision for Lamberts Dalston, Ltd. (Luton, Beds.) in 1988: 1 original PMA approval. All are in product code LLQ (Cap, Cervical, Contraceptive). 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 Lamberts Dalston, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Lamberts Dalston, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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