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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 12 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | 10MRRL | FDA UDI | Class II | Active |
| Endoplus | E347MR | FDA UDI | Class II | Active |
| Endoplus | 10441 | FDA UDI | Class II | Active |
| Endoplus | E345R | FDA UDI | Class II | Active |
| Endoplus | E369R | FDA UDI | Class II | Active |
| Endoplus | E347AC | FDA UDI | Class II | Active |
| Endoplus | E346SLR-37 | FDA UDI | Class II | Active |
| Endoplus | E318RR | FDA UDI | Class II | Active |
| Endoplus | E327S | FDA UDI | Class II | Active |
| Endoplus | 5XFR | FDA UDI | Class II | Unknown |
| Endoplus | E437AC | FDA UDI | Class II | Active |
| Endoplus | 5SLRL | FDA UDI | Class II | Active |
| Endoplus | E348SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E335SLR | FDA UDI | Class II | Active |
| Endoplus | E349M | FDA UDI | Class II | Active |
| Endoplus | E431SLR | FDA UDI | Class II | Active |
| Endoplus | E306MR | FDA UDI | Class II | Active |
| Endoplus | E420ACR | FDA UDI | Class II | Active |
| Endoplus | E342SLR | FDA UDI | Class II | Active |
| Endoplus | 5355 | FDA UDI | Class II | Active |
| Endoplus | E376MR | FDA UDI | Class II | Active |
| Endoplus | 345VA | FDA UDI | Class II | Active |
| Endoplus | 10416L | FDA UDI | Class II | Active |
| Endoplus | E316MR | FDA UDI | Class II | Active |
| Endoplus | E300DVR-45 | FDA UDI | Class II | Active |
| Endoplus | EN706 | FDA UDI | Class II | Active |
| Endoplus | 5356L | FDA UDI | Class II | Active |
| Endoplus | E307RR-45 | FDA UDI | Class II | Active |
| Endoplus | E364SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E347SR | FDA UDI | Class II | Active |
| Endoplus | 10404 | FDA UDI | Class II | Active |
| Endoplus | 5XRR | FDA UDI | Class II | Active |
| Endoplus | E377RR-45 | FDA UDI | Class II | Active |
| Endoplus | EN306-45 | FDA UDI | Class II | Active |
| Endoplus | 5376 | FDA UDI | Class II | Active |
| Endoplus | 5330 | FDA UDI | Class II | Active |
| Endoplus | E389MR | FDA UDI | Class II | Active |
| Endoplus | E320M | FDA UDI | Class II | Active |
| Endoplus | E313RR | FDA UDI | Class II | Active |
| Endoplus | 5327L | FDA UDI | Class II | Active |
| Endoplus | E328SLR | FDA UDI | Class II | Active |
| Endoplus | E322RR | FDA UDI | Class II | Active |
| Endoplus | 10SLRL | FDA UDI | Class II | Active |
| Endoplus | EN803L | FDA UDI | Class II | Active |
| Endoplus | E437R | FDA UDI | Class II | Active |
| Endoplus | E364S | FDA UDI | Class II | Active |
| Endoplus | EN308L | FDA UDI | Class II | Active |
| Endoplus | E345SLR-45 | FDA UDI | Class II | Active |
| Endoplus | 5389 | FDA UDI | Class II | Active |
| Endoplus | E375RR | 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. |