FDA applicant
Albyn Medical, Ltd.
FDA records 1 decision for Albyn Medical, Ltd. (Dingwall, Ross-Shire, GB) in 1997: 1 510(k) clearance. All are in product code EXY (Uroflowmeter). 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 Albyn Medical, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Albyn Medical, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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