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PHENOX LIMITED

US

Last updated May 24, 2026

Part of phenox GmbH

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
985621869

Catalogue (18)

DeviceModel / ReferenceRegistriesClassStatus
pRESET® Delta LITE Thrombectomy Device (3mm x 20mm) PRE2-LT-3-20
FDA UDI
Class IIActive
pRESET® Delta LITE Thrombectomy Device (4mm x 20mm) PRE2-LT-4-20
FDA UDI
Class IIActive
pORTAL® Steerable Hydrophilic Guidewire PORT-14-200-1
FDA UDI
Class IIActive
pRESET® LITE Thrombectomy Device (3mm x 20mm) PRE-LT-3-20
FDA UDI
Class IIActive
pNOVUS 21 Microcatheter (150cm) PNOV-21-150
FDA UDI
Class IIActive
pRESET® Thrombectomy Device (5mm x 40mm) PRE-5-40
FDA UDI
Class IIActive
pRESET® LITE Thrombectomy Device (4mm x 20mm) PRE-LT-4-20
FDA UDI
Class IIActive
pNOVUS 21 Microcatheter (160cm) PNOV-21-160
FDA UDI
Class IIActive
pRESET® Delta Thrombectomy Device (4mm x 20mm) PRE2-4-20
FDA UDI
Class IIActive
pRESET® Thrombectomy Device (6mm x 30mm) PRE-6-30
FDA UDI
Class IIActive
pRESET® Delta Thrombectomy Device (6mm x 30mm) PRE2-6-30
FDA UDI
Class IIActive
pORTAL® EXT Extension Wire PORT-14-115-1-EX
FDA UDI
Class IIActive
pNOVUS 21 Microcatheter PNOV-21-160
FDA UDI
Class IIActive
pRESET® Thrombectomy Device (4mm x 20mm) PRE-4-20
FDA UDI
Class IIActive
pRESET® Delta Thrombectomy Device (5mm x 40mm) PRE2-5-40
FDA UDI
Class IIActive
pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device K242676
FDA 510(k)
Class IIActive
pORTAL Steerable Hydrophilic Guidewire and pORTAL EXT Extension Wire K191687
FDA 510(k)
Class IIActive
pRESET LITE Thrombectomy Device K231539
FDA 510(k)
Class IIActive

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