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Sign in to claim this brandEndoplus
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 750 Tower Rd Ste A, Mundelein, IL, 60060
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3000719482
- DUNS Number
- 794679167
Catalogue (902)
Page 17 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E339R | FDA UDI | Class II | Active |
| Endoplus | 10424L | FDA UDI | Class II | Active |
| Endoplus | E300M | FDA UDI | Class II | Active |
| Endoplus | E369DVR | FDA UDI | Class II | Active |
| Endoplus | 10MRL | FDA UDI | Class II | Active |
| Endoplus | 5850 | FDA UDI | Class II | Active |
| Endoplus | E402RR-45 | FDA UDI | Class II | Active |
| Endoplus | 312VA | FDA UDI | Class II | Active |
| Endoplus | E317SL | FDA UDI | Class II | Active |
| Endoplus | E382SR-45 | FDA UDI | Class II | Active |
| Endoplus | E307SR | FDA UDI | Class II | Active |
| Endoplus | 5322L | FDA UDI | Class II | Active |
| Endoplus | 5554L | FDA UDI | Class II | Active |
| Endoplus | 5347L | FDA UDI | Class II | Active |
| Endoplus | 5312L | FDA UDI | Class II | Active |
| Endoplus | EN702 | FDA UDI | Class II | Active |
| Endoplus | E363SR | FDA UDI | Class II | Active |
| Endoplus | 327VA | FDA UDI | Class II | Active |
| Endoplus | E331DVR-45 | FDA UDI | Class II | Active |
| Endoplus | E430RR | FDA UDI | Class II | Active |
| Endoplus | E321R | FDA UDI | Class II | Active |
| Endoplus | E307DVR-45 | FDA UDI | Class II | Active |
| Endoplus | 10412 | FDA UDI | Class II | Active |
| Endoplus | E346RR | FDA UDI | Class II | Active |
| Endoplus | E347M | FDA UDI | Class II | Active |
| Endoplus | 5355L | FDA UDI | Class II | Active |
| Endoplus | 5346J | FDA UDI | Class II | Active |
| Endoplus | EN701L | FDA UDI | Class II | Active |
| Endoplus | E396DVR-45 | FDA UDI | Class II | Active |
| Endoplus | E345AC-45 | FDA UDI | Class II | Active |
| Endoplus | E355DVR-45 | FDA UDI | Class II | Active |
| Endoplus | E301SR | FDA UDI | Class II | Active |
| Endoplus | E369R-45 | FDA UDI | Class II | Active |
| Endoplus | 5319 | FDA UDI | Class II | Active |
| Endoplus | E424DVR | FDA UDI | Class II | Active |
| Endoplus | EN804L | FDA UDI | Class II | Active |
| Endoplus | E307RR | FDA UDI | Class II | Active |
| Endoplus | EN706L | FDA UDI | Class II | Active |
| Endoplus | 5310L | FDA UDI | Class II | Active |
| Endoplus | E333R | FDA UDI | Class II | Active |
| Endoplus | E361S | FDA UDI | Class II | Active |
| Endoplus | E329M | FDA UDI | Class II | Active |
| Endoplus | E325MR | FDA UDI | Class II | Active |
| Endoplus | 5309L | FDA UDI | Class II | Active |
| Endoplus | 5377L | FDA UDI | Class II | Active |
| Endoplus | E341SLR | FDA UDI | Class II | Active |
| Endoplus | E364AC | FDA UDI | Class II | Active |
| Endoplus | E374SLR | FDA UDI | Class II | Active |
| Endoplus | 5367 | FDA UDI | Class II | Active |
| Endoplus | E301RR | FDA UDI | Class II | Active |
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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jul 15, 2013 | Z-2265-2013 | — | terminated | Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. |
| Jul 15, 2013 | Z-2264-2013 | — | terminated | Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. |