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Endoplus

US

Last updated September 17, 2026

Information

Country
US
Address
750 Tower Rd Ste A, Mundelein, IL, 60060
Website
—
LinkedIn
—
Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
3000719482
DUNS Number
794679167

Catalogue (902)

Page 3 of 19
DeviceModel / ReferenceRegistriesClassStatus
Endoplus E322DVR-45
FDA UDI
Class IIActive
Endoplus 5335L
FDA UDI
Class IIActive
Endoplus E300DVR
FDA UDI
Class IIActive
Endoplus 5MFRR
FDA UDI
Class IIActive
Endoplus 5317L
FDA UDI
Class IIActive
Endoplus 5345
FDA UDI
Class IIActive
Endoplus 5FR
FDA UDI
Class IIActive
Endoplus E414RR
FDA UDI
Class IIActive
Endoplus E346SR-37
FDA UDI
Class IIActive
Endoplus E333ACR-37
FDA UDI
Class IIActive
Endoplus E337MR
FDA UDI
Class IIActive
Endoplus E348RR
FDA UDI
Class IIActive
Endoplus E323RR
FDA UDI
Class IIActive
Endoplus E339RR
FDA UDI
Class IIActive
Endoplus E341M
FDA UDI
Class IIActive
Endoplus E304MR-45
FDA UDI
Class IIActive
Endoplus 347VL
FDA UDI
Class IIActive
Endoplus E330RR
FDA UDI
Class IIActive
Endoplus E369SR-45
FDA UDI
Class IIActive
Endoplus CF-369L
FDA UDI
Class IIActive
Endoplus E370RR
FDA UDI
Class IIActive
Endoplus E375SLR
FDA UDI
Class IIActive
Endoplus 5378L
FDA UDI
Class IIActive
Endoplus E333RR
FDA UDI
Class IIActive
Endoplus E378SR
FDA UDI
Class IIActive
Endoplus E364SL
FDA UDI
Class IIActive
Endoplus E367DVR
FDA UDI
Class IIActive
Endoplus 5394
FDA UDI
Class IIActive
Endoplus E375MR-45
FDA UDI
Class IIActive
Endoplus 341VA
FDA UDI
Class IIActive
Endoplus 5553L
FDA UDI
Class IIActive
Endoplus E347R-45
FDA UDI
Class IIActive
Endoplus E345SL-45
FDA UDI
Class IIActive
Endoplus E302R
FDA UDI
Class IIActive
Endoplus E331MR-45
FDA UDI
Class IIActive
Endoplus E369SLR-45
FDA UDI
Class IIActive
Endoplus E424DVR-45
FDA UDI
Class IIActive
Endoplus E404SLR
FDA UDI
Class IIActive
Endoplus E317MR-37
FDA UDI
Class IIActive
Endoplus E349RR
FDA UDI
Class IIActive
Endoplus E417R
FDA UDI
Class IIActive
Endoplus 10434L
FDA UDI
Class IIActive
Endoplus E345MR
FDA UDI
Class IIActive
Endoplus 5650L
FDA UDI
Class IIActive
Endoplus E327MR
FDA UDI
Class IIActive
Endoplus E327SR
FDA UDI
Class IIActive
Endoplus E347DVR-45
FDA UDI
Class IIActive
Endoplus E324SLR
FDA UDI
Class IIActive
Endoplus 5325
FDA UDI
Class IIActive
Endoplus 10402
FDA UDI
Class IIActive

Related Companies

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Authorities

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FDA Recalls (2)

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 15, 2013Z-2265-2013—terminated

Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.

Jul 15, 2013Z-2264-2013—terminated

Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.