FDA applicant
Duckworth & Kent, Ltd.
FDA records 6 decisions for Duckworth & Kent, Ltd. (Baldock, Hertfordshire, GB) from 2003 to 2008: 6 510(k) clearances. Most are in product codes MSS (Folders And Injectors, Intraocular Lens (Iol)) and KYB (Lens, Guide, Intraocular). 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 Duckworth & Kent, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2008
2007high 2 (2008) · low 0 (2007)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Duckworth & Kent, Ltd.’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