FDA applicant
Exmoor Plastics, Ltd.
FDA records 43 decisions for Exmoor Plastics, Ltd. (Taunton, GB) from 1981 to 2010: 43 510(k) clearances. Most are in product codes ETD (Tube, Tympanostomy) and LRC (Instrument, Ent Manual Surgical). Its devices cite 4 predicates, 3 of them its own earlier devices. 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 Exmoor Plastics, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2010
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Exmoor Plastics, 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