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Phenox Limited

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device (K242676)Phenox Limited2025-02-28
pRESET LITE Thrombectomy Device (K231539)Phenox Limited2023-10-21
pRESET Thrombectomy Device (K222848)Phenox Limited2023-01-20
pORTAL Steerable Hydrophilic Guidewire and pORTAL EXT Extension Wire (K191687)Phenox Limited2019-10-09

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Every clearance here is in the API, with alerts when new ones post.