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Edwards Lifesciences LLC

US

Last updated September 17, 2026

What Edwards Lifesciences LLC makes

Edwards Lifesciences LLC manufactures single-use and reusable invasive-pressure transducers, electrical connection cables, and arterial blood sampling kits for clinical monitoring. Their portfolio includes open-surgery and transcatheter aortic heart valves, cardiopulmonary bypass cannulae for drainage and return, and pulmonary artery balloon catheters with electrical functionality. Additional products include retrograde cardioplegia catheters, femoral arterial cannulae, and continuous cardiac output monitoring sensors.

The company’s devices are classified under FDA categories Class I, Class II, and Class III, with listings in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
ONE EDWARDS WAY, IRVINE, CA, 92614
Website
edwards.com
LinkedIn
—
Facebook
—
Phone
+1(800)822-9637
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
2015691
DUNS Number
134139174

Catalogue (1779)

Page 7 of 36
DeviceModel / ReferenceRegistriesClassStatus
Truwave, Vamp PXVK0388
FDA UDI
Class IIActive
Fogarty 620403F
FDA UDI
Class IIActive
Truwave T001758A
FDA UDI
Class IIActive
Thin-Flex Single Stage Malleable Venous Drainage Cannula TFM024L
FDA UDI
Class IIUnknown
Truwave PXMK1915
FDA UDI
Class IIActive
Clearsight CSCM
FDA UDI
Class IIActive
Truwave VLMFV150
FDA UDI
Class IIActive
Edwards Lifesciences Retrograde Cardioplegia Catheter RC014I
FDA UDI
Class IIActive
Percutaneous Insertion Kit-Arterial PIKA
FDA UDI
Class IIActive
Truwave, Vamp Plus PXVP0861
FDA UDI
Class IIActive
Truwave X 3 (3 Cc) /vamp 75 In (190 Cm) T430140A
FDA UDI
Class IIActive
Truwave X 2 (3 Cc) /vamp 78 In (200 Cm) T005049B
FDA UDI
Class IIActive
Edwards Lifesciences Aortic Perfusion Cannula PAA010CB
FDA UDI
Class IIUnknown
Truwave PXMK2306
FDA UDI
Class IIActive
HemoSphere Vita HEMVEXPM1
FDA UDI
Class IIActive
Truwave PXMK2047
FDA UDI
Class IIActive
Truwave T333919A
FDA UDI
Class IIActive
Truwave T001712A
FDA UDI
Class IIActive
Edwards Oximetry Central Venous Catheter X3820KT
FDA UDI
Class IIActive
Truwave, Vamp Plus PXVP0880
FDA UDI
Class IIActive
Truwave PXMK1976
FDA UDI
Class IIActive
Fogarty Corkscrew 1408010
FDA UDI
Class IIActive
Truwave PXMK1882
FDA UDI
Class IIActive
Vamp Jr. VMP406
FDA UDI
Class IIActive
Truwave PXMK1183
FDA UDI
Class IIActive
Truwave, Vamp Plus T430023M
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Hemosphere HEMPSC100
FDA UDI
Class IIActive
Truwave PXMK1505
FDA UDI
Class IIActive
Fogarty 220806F
FDA UDI
Class IActive
Truwave PXAK2066
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Flotrac, Vamp, Truwave MHD6C502
FDA UDI
Class IIActive
Truwave PXMK1978
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Vamp VK1074
FDA UDI
Class IIActive
Vamp Plus VP2
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Truwave T001709A
FDA UDI
Class IIActive
Carpentier-Edwards Duraflex Bioprosthesis - Mitral 6625-ESR-LP
FDA UDI
Class IIIActive
Fogarty 62080814F
FDA UDI
Class IIActive
Edwards Lifesciences Dispersion Aortic Perfusion Cannula DCT21TA
FDA UDI
Class IIActive
TruWave PXVPZ10025
FDA UDI
Class IIActive
Flex-Tip D98500
FDA UDI
Class IIActive
Co-Set Injectate Ice Bucket 93520
FDA UDI
Class IIActive
Truwave, Vamp Plus PXVP23X3
FDA UDI
Class IIActive
Vamp 48AVMP
FDA UDI
Class IIActive
AViD Dual Stage Venous Drainage Cannula TF293702A
FDA UDI
Class IIActive
Truwave X 2 (3 Cc) /vamp 78 In (200 Cm) T440B26B
FDA UDI
Class IIActive
Swan-Ganz Hi-Shore True Size 141F7
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Jul 31, 2015Z-2776-2015—terminated

Flow restriction issues in a trifurcated IV set included in the pressure transducer kits. A restriction of the flow of IV fluid would result in either an inability to prime the system before use or difficulty in flushing the line after a blood draw.

FDA Establishments (2)

Establishments registered with the FDA under this company group, matched by name.

  • Edwards Lifesciences Guadalupe Cartago · CR FEI 3015287573
  • Edwards Lifesciences LTD Shannon Clare · IE FEI 3015179394