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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 25 of 36
DeviceModel / ReferenceRegistriesClassStatus
Carpentier-Edwards Perimount Magna Mitral Pericardial Bioprosthesis 7000TFX
FDA UDI
Class IIIActive
Edwards Sapien 3 Transcatheter Heart Valve (thv) 9600TFX
FDA UDI
Class IIIActive
Thin-Flex Single Stage Malleable Venous Drainage Cannula TFM036L
FDA UDI
Class IIUnknown
Edwards Intuity Elite Valve System 8300KITB19
FDA UDI
Class IIIActive
Acumen Iq Sensor AIQS6AZ5
FDA UDI
Class IIActive
Fogarty 120602F
FDA UDI
Class IIActive
Fogarty 12TLW805F35
FDA UDI
Class IIActive
Truwave, Vamp PXVK1001
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
EMBOL-X Intra-Aortic Filter with Duraflo Coating EXXSD
FDA UDI
Class IIActive
Edwards 10000UP
FDA UDI
Class IActive
Truwave PXMK1977
FDA UDI
Class IIActive
Carpentier-Edwards Physio Ii Annuloplasty Ring 5200
FDA UDI
Class IIActive
Truwave, Vamp Jr. VMP306PX
FDA UDI
Class IIActive
Truwave 896632004
FDA UDI
Class IIActive
Fogarty 12TLW806F
FDA UDI
Class IIActive
Swan-Ganz True Size S111F7
FDA UDI
Class IIActive
Truwave 896494023
FDA UDI
Class IIActive
SAPIEN 3 Ultra System 9750CM20
FDA UDI
Class IIIActive
Carpentier-Edwards Perimount Rsrpericardial Bioprosthesis - Aortic 2800
FDA UDI
Class IIIActive
Truwave X 3 (3 Cc)/Vamp Plus (215 Cm) T100671M
FDA UDI
Class IIActive
Truwave PX600I
FDA UDI
Class IIActive
Truwave, Vamp PXVK0738
FDA UDI
Class IIActive
VAMP Optima VOPTIMA
FDA UDI
Class IIActive
Truwave T001789B
FDA UDI
Class IIActive
Carpentier-Edwards Classic Annuloplasty Ring - Mitral 4400
FDA UDI
Class IIActive
23mm X 4cm X 130cm Edwards Balloon Catheter 9350BC23
FDA UDI
Class IIActive
Truwave PXMK1289
FDA UDI
Class IIActive
ForeSight FSESNS
FDA UDI
Class IIActive
Carpentier-Edwards Bioprosthesis - Aortic 2625
FDA UDI
Class IIIActive
MITRIS RESILIA Mitral Valve 11400M
FDA UDI
Class IIIActive
TruWave, VAMP Plus PXVPL0113
FDA UDI
Class IIActive
Acumen Iq AIQFM10
FDA UDI
Class IIActive
Truwave PXMK1749
FDA UDI
Class IIActive
Edwards Lifesciences Vent Catheter E063
FDA UDI
Class IIActive
Truwave 50P160
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
PX1800 – Truwave Cables 896634002
FDA UDI
Class IIActive
Truwave PX1800
FDA UDI
Class IIActive
HemoSphere Vita HEMVITA1
FDA UDI
Class IIActive
Truwave T001797B
FDA UDI
Class IIActive
Truwave, Vamp PXVK0995
FDA UDI
Class IIActive
Truwave PXMK9146
FDA UDI
Class IIActive
Truwave PX200
FDA UDI
Class IIActive
SAPIEN 3 Ultra delivery system 9630TF29
FDA UDI
Class IIIActive
Ev1000 Table Stand EVS1
FDA UDI
Class IIActive
Carpentier-Edwards Classic Annuloplasty Ring - Mitral 4400
FDA UDI
Class IIActive
Swan-Ganz Controlcath C146F7
FDA UDI
Class IIActive
Carpentier-Edwards Physio Annuloplasty Ring With Holder - Mitral 4450
FDA UDI
Class IIActive
Heart Valve Accessor 1117
FDA UDI
Class IActive

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