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Endoplus

US

Last updated September 17, 2026

Information

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

Catalogue (902)

Page 19 of 19
DeviceModel / ReferenceRegistriesClassStatus
Endoplus E304SLR
FDA UDI
Class IIActive
ENDOPLUS hand-held laparoscopic instruments K151567
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

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.