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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 1 of 19
DeviceModel / ReferenceRegistriesClassStatus
Endoplus 5375
FDA UDI
Class IIActive
Endoplus E328MR
FDA UDI
Class IIActive
Endoplus E308RR-45
FDA UDI
Class IIActive
Endoplus E377RR
FDA UDI
Class IIActive
Endoplus E333RR-37
FDA UDI
Class IIActive
Endoplus 5552
FDA UDI
Class IIActive
Endoplus 5SLR
FDA UDI
Class IIActive
Endoplus 5150L
FDA UDI
Class IIActive
Endoplus 5321L
FDA UDI
Class IIActive
Endoplus E373MR
FDA UDI
Class IIActive
Endoplus E313MR
FDA UDI
Class IIActive
Endoplus 5363
FDA UDI
Class IIActive
Endoplus 336VL
FDA UDI
Class IIActive
Endoplus E434RR
FDA UDI
Class IIActive
Endoplus E337RR-45
FDA UDI
Class IIActive
Endoplus E338RR
FDA UDI
Class IIActive
Endoplus E321MR-45
FDA UDI
Class IIActive
Endoplus 5553
FDA UDI
Class IIActive
Endoplus EN800L
FDA UDI
Class IIActive
Endoplus E420RR-45
FDA UDI
Class IIActive
Endoplus 317VA
FDA UDI
Class IIActive
Endoplus EN303
FDA UDI
Class IIActive
Endoplus 5326
FDA UDI
Class IIActive
Endoplus E340SLR
FDA UDI
Class IIActive
Endoplus 5340L
FDA UDI
Class IIActive
Endoplus E327SLR
FDA UDI
Class IIActive
Endoplus E338R
FDA UDI
Class IIActive
Endoplus E342M
FDA UDI
Class IIActive
Endoplus 5374L
FDA UDI
Class IIActive
Endoplus 5346L
FDA UDI
Class IIActive
Endoplus E307DVR
FDA UDI
Class IIActive
Endoplus 10RR
FDA UDI
Class IIActive
Endoplus E363RR
FDA UDI
Class IIActive
Endoplus E344MR
FDA UDI
Class IIActive
Endoplus E323SLR-45
FDA UDI
Class IIActive
Endoplus su5652L
FDA UDI
Class IIActive
Endoplus E342SR
FDA UDI
Class IIActive
Endoplus E369DVR-45
FDA UDI
Class IIActive
Endoplus E302SL
FDA UDI
Class IIActive
Endoplus E318MR
FDA UDI
Class IIActive
Endoplus E336RR
FDA UDI
Class IIActive
Endoplus E328RR
FDA UDI
Class IIActive
Endoplus E333SLR-37
FDA UDI
Class IIActive
Endoplus EN301-45
FDA UDI
Class IIActive
Endoplus E336SLR-45
FDA UDI
Class IIActive
Endoplus EN320-45
FDA UDI
Class IIActive
Endoplus 5348L
FDA UDI
Class IIActive
Endoplus E333SLR-32
FDA UDI
Class IIActive
Endoplus 5344L
FDA UDI
Class IIActive
Endoplus E335SR-45
FDA UDI
Class IIActive

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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.