Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Endoplus

US

Last updated September 17, 2026

Information

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

Catalogue (902)

Page 7 of 19
DeviceModel / ReferenceRegistriesClassStatus
Endoplus E388M
FDA UDI
Class IIActive
Endoplus E446SR
FDA UDI
Class IIActive
Endoplus E370AC
FDA UDI
Class IIActive
Endoplus 5SLFRJ
FDA UDI
Class IIActive
Endoplus 5330L
FDA UDI
Class IIActive
Endoplus 5361
FDA UDI
Class IIActive
Endoplus E437SR
FDA UDI
Class IIActive
Endoplus E342RR
FDA UDI
Class IIActive
Endoplus E347M-25
FDA UDI
Class IIActive
Endoplus EN400
FDA UDI
Class IIActive
Endoplus E362AC
FDA UDI
Class IIActive
Endoplus E300SLR
FDA UDI
Class IIActive
Endoplus E321AC-45
FDA UDI
Class IIActive
Endoplus E346DVR
FDA UDI
Class IIActive
Endoplus 10SLR
FDA UDI
Class IIActive
Endoplus E329MR
FDA UDI
Class IIActive
Endoplus 10414L
FDA UDI
Class IIActive
Endoplus E356SLR
FDA UDI
Class IIActive
Endoplus ES0507RR-45
FDA UDI
Class IIActive
Endoplus E369SR-25
FDA UDI
Class IIActive
Endoplus SLRVL
FDA UDI
Class IIActive
Endoplus E315M
FDA UDI
Class IIActive
Endoplus E338DVR-45
FDA UDI
Class IIActive
Endoplus E366DVR-45
FDA UDI
Class IIActive
Endoplus 10417L
FDA UDI
Class IIActive
Endoplus E333SL-37
FDA UDI
Class IIActive
Endoplus E369S
FDA UDI
Class IIActive
Endoplus 5370
FDA UDI
Class IIActive
Endoplus 5331L
FDA UDI
Class IIActive
Endoplus E346AC
FDA UDI
Class IIActive
Endoplus E330SLR
FDA UDI
Class IIActive
Endoplus E304RR
FDA UDI
Class IIActive
Endoplus 5300
FDA UDI
Class IIActive
Endoplus 5396
FDA UDI
Class IIActive
Endoplus ES0507RR
FDA UDI
Class IIActive
Endoplus E368RR
FDA UDI
Class IIActive
Endoplus E329M-45
FDA UDI
Class IIActive
Endoplus su5650L
FDA UDI
Class IIActive
Endoplus E306R
FDA UDI
Class IIActive
Endoplus E327M
FDA UDI
Class IIActive
Endoplus E432RR-45
FDA UDI
Class IIActive
Endoplus 5305
FDA UDI
Class IIActive
Endoplus E364R
FDA UDI
Class IIActive
Endoplus E317DVR
FDA UDI
Class IIActive
Endoplus E311SR
FDA UDI
Class IIActive
Endoplus 5MRRJ
FDA UDI
Class IIActive
Endoplus 5MRC
FDA UDI
Class IIActive
Endoplus 5366L
FDA UDI
Class IIActive
Endoplus EN308
FDA UDI
Class IIActive
Endoplus E412R
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 (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.