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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 3 of 36
DeviceModel / ReferenceRegistriesClassStatus
PX1800 – Truwave Cables 896632002
FDA UDI
Class IIActive
Edwards Crimper 9600CR
FDA UDI
Class IIIActive
Truwave, Vamp PXVK220
FDA UDI
Class IIActive
Swan-Ganz 177F75N
FDA UDI
Class IIActive
Truwave Cables PX1800
FDA UDI
Class IIActive
Truwave PXCMK590
FDA UDI
Class IIActive
Truwave PXAK2422
FDA UDI
Class IIActive
Truwave PXMK2160
FDA UDI
Class IIActive
Co-Set+ 93524
FDA UDI
Class IIActive
20mm X 4cm X 130cm Edwards Balloon Catheter 9350BC20
FDA UDI
Class IIActive
Pascal 20000ISM
FDA UDI
Class IIIActive
AViD Dual Stage Venous Drainage Cannula TF293702
FDA UDI
Class IIActive
Truwave PXMK1085
FDA UDI
Class IIActive
Carpentier-Edwards Perimount Theon Pericardialbioprosthesis - Mitral 6900PTFX
FDA UDI
Class IIIActive
FloTrac IQ sensor MHDQ6AZ
FDA UDI
Class IIActive
EMBOL-X Intra-Aortic Filter with Duraflo Coating EXSSD
FDA UDI
Class IIActive
Fogarty 12A0803F
FDA UDI
Class IIActive
Truwave PX2X2YB
FDA UDI
Class IIActive
Edwards Lifesciences Aortic Perfusion Cannula ARH221190TA
FDA UDI
Class IIActive
Truwave 50P112
FDA UDI
Class IIActive
Flotrac MHD8S102
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Truwave T331U03C
FDA UDI
Class IIActive
Truwave, Vamp PXVK1079
FDA UDI
Class IIActive
Carpentier-Edwards Bioprosthetic Valved Conduit 4300
FDA UDI
Class IIIActive
TruWave, VAMP Plus PXVPL2284
FDA UDI
Class IIActive
Carpentier-Edwards Perimount Plus Pericardial Bioprosthesis - Mitral 6900P
FDA UDI
Class IIIActive
Truwave PXMK500
FDA UDI
Class IIUnknown
Pascal 20000IS
FDA UDI
Class IIIActive
Fem-Flex Femoral Arterial Cannula TFA02425H
FDA UDI
Class IIActive
A Handle Compatible With Ring Holders Models 5100, 4900, 4100, 4200, 4450 And 46 1151
FDA UDI
Class IActive
PX1800 – Truwave Cables 896625022
FDA UDI
Class IIActive
Edwards Lifesciences EZ Glide Aortic Cannula EZC24TA
FDA UDI
Class IIActive
Edwards Lifesciences Aortic Perfusion Cannula AA022TF
FDA UDI
Class IIUnknown
PX1800 – Truwave Cables 896639002
FDA UDI
Class IIActive
Truwave PX3X3284C
FDA UDI
Class IIActive
Truwave T328201A
FDA UDI
Class IIActive
Vamp Plus VP181Z
FDA UDI
Class IIActive
Thin-Flex Dual Stage Venous Drainage Cannula TF2020O
FDA UDI
Class IIActive
Vamp Plus VP1
FDA UDI
Class IIActive
Ascendra Balloon Aortic Valvuloplasty Catheter 9100BAVC
FDA UDI
Class IIActive
Truwave (3 Cc) /vamp 78 In (200 Cm) T440B28A
FDA UDI
Class IIActive
Edwards Detlogix Annuloplasty Ring 5100
FDA UDI
Class IIActive
VolumeView VLV8R520
FDA UDI
Class IIActive
Geoform Annuloplasty Ring With Holder - Mitral 4200
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Truwave MK2260
FDA UDI
Class IIActive
PX1800 – Truwave Cables 896019029
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Vamp Jr. VMP306
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