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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 26 of 36
DeviceModel / ReferenceRegistriesClassStatus
PX1800 – Truwave Cables 896639004
FDA UDI
Class IIActive
Fogarty Safejaw DSAFE86
FDA UDI
Class IIActive
Edwards Lifesciences Retrograde Cardioplegia Catheter RC2014S
FDA UDI
Class IIActive
Heart Valve Accessor 1150
FDA UDI
Class IActive
Truwave MFNVC
FDA UDI
Class IIActive
Edwards Lifesciences Aortic Perfusion Cannula AAS022TFA
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Truwave PXMK1132
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Edwards Sapien Xt Transcatheter Heart Valve (thv) 9300TFX
FDA UDI
Class IIIActive
Truwave, Vamp Plus PXVP0686
FDA UDI
Class IIActive
Truwave T005025A
FDA UDI
Class IIActive
Edwards Commander Delivery System 9600LDS23
FDA UDI
Class IIIActive
Truwave, Vamp Jr. PXVJ0711
FDA UDI
Class IIActive
Truwave T333918A
FDA UDI
Class IIActive
Truwave 896612022
FDA UDI
Class IIActive
Truwave PXMK0695
FDA UDI
Class IIActive
Edwards Commander Delivery System 9600LDS26
FDA UDI
Class IIIActive
Fogarty 410405FP
FDA UDI
Class IIActive
Swan-Ganz Ccombo 746F8
FDA UDI
Class IIActive
Carpentier-Edwards Classic Annuloplasty Ring - Tricuspid 4500T
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
Edwards Oximetry Central Venous Catheter X3816ST
FDA UDI
Class IIActive
Konect Resilia 11060A
FDA UDI
Class IIIActive
Truwave T001657A
FDA UDI
Class IIActive
Fem-Flex II Femoral Arterial Cannula FEMII016AS
FDA UDI
Class IIActive
Co-Set+ 93528
FDA UDI
Class IIActive
Edwards Intuity Elite Aortic Valve 8300AB
FDA UDI
Class IIIActive
HemoSphere Vita HEMVLTECHM1
FDA UDI
Class IIActive
Truwave T330V11A
FDA UDI
Class IIActive
Truwave PX212
FDA UDI
Class IIActive
Swan-Ganz Pacing Td Catheter D205F7
FDA UDI
Class IIActive
Flexible Handle 1173
FDA UDI
Class IActive
Truwave, Vamp Plus PXVP1071
FDA UDI
Class IIActive
Fogarty 120403F
FDA UDI
Class IIActive
FemTrak Femoral Venous Cannula FTV020
FDA UDI
Class IIActive
Edwards Prima Plus Stentless Bioprosthesis - Aortic 2500P
FDA UDI
Class IIIActive
Truwave PXMK2144
FDA UDI
Class IIActive
PX1800 – Truwave Cables 896034025
FDA UDI
Class IIActive
EMBOL-X Glide Access Device/Aortic Cannula with Flange EXGF24D
FDA UDI
Class IIActive
Truwave 50P172
FDA UDI
Class IIActive
Fogarty Safejaw-Hydrajaw SAFEHY33
FDA UDI
Class IIActive
AViD Dual Stage Venous Drainage Cannula TF292902A
FDA UDI
Class IIActive
Acumen IQ Fluid Meter AIQFM
FDA UDI
Class IIActive
Swan-Ganz Vip 831VF75P
FDA UDI
Class IIActive
Inspiris Resilia Aortic Valve 11500A
FDA UDI
Class IIIActive
Truwave T333F00A
FDA UDI
Class IIActive
Edwards Intuity Elite Delivery System 8300DB19
FDA UDI
Class IIIActive
Edwards Oximetry Central Venous Catheter XA3820SAFKT
FDA UDI
Class IIActive
Thin-Flex Single Stage Venous Drainage Cannula TF028L90
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