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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 13 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | 5341 | FDA UDI | Class II | Active |
| Endoplus | 5328L | FDA UDI | Class II | Active |
| Endoplus | E304RR-45 | FDA UDI | Class II | Active |
| Endoplus | 5306L | FDA UDI | Class II | Active |
| Endoplus | 10RL | FDA UDI | Class II | Active |
| Endoplus | E362SR | FDA UDI | Class II | Active |
| Endoplus | E420SR | FDA UDI | Class II | Active |
| Endoplus | E343MR | FDA UDI | Class II | Active |
| Endoplus | E336R | FDA UDI | Class II | Active |
| Endoplus | 5369 | FDA UDI | Class II | Active |
| Endoplus | E346SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E302RR | FDA UDI | Class II | Active |
| Endoplus | E437RR | FDA UDI | Class II | Active |
| Endoplus | E366DVR | FDA UDI | Class II | Active |
| Endoplus | 304VA | FDA UDI | Class II | Active |
| Endoplus | 5316L | FDA UDI | Class II | Active |
| Endoplus | E327AC | FDA UDI | Class II | Active |
| Endoplus | 323VL | FDA UDI | Class II | Active |
| Endoplus | E344SR-45 | FDA UDI | Class II | Active |
| Endoplus | E301RR-45 | FDA UDI | Class II | Active |
| Endoplus | E312MR | FDA UDI | Class II | Active |
| Endoplus | E432R | FDA UDI | Class II | Active |
| Endoplus | E323SR-45 | FDA UDI | Class II | Active |
| Endoplus | E346SL-45 | FDA UDI | Class II | Active |
| Endoplus | 5381L | FDA UDI | Class II | Active |
| Endoplus | 5MRSL | FDA UDI | Class II | Active |
| Endoplus | E337SLR | FDA UDI | Class II | Active |
| Endoplus | E315MR-22 | FDA UDI | Class II | Active |
| Endoplus | 327VL | FDA UDI | Class II | Active |
| Endoplus | 5311 | FDA UDI | Class II | Active |
| Endoplus | E300RR | FDA UDI | Class II | Active |
| Endoplus | 5MRRCL | FDA UDI | Class II | Active |
| Endoplus | E420DVR | FDA UDI | Class II | Active |
| Endoplus | 5550L | FDA UDI | Class II | Active |
| Endoplus | EN703 | FDA UDI | Class II | Active |
| Endoplus | E434ACR | FDA UDI | Class II | Active |
| Endoplus | 5R | FDA UDI | Class II | Active |
| Endoplus | 5MFR | FDA UDI | Class II | Active |
| Endoplus | 5750L | FDA UDI | Class II | Active |
| Richard Wolf | 89.944 | FDA UDI | Class II | Active |
| Endoplus | 5336 | FDA UDI | Class II | Active |
| Endoplus | 5356 | FDA UDI | Class II | Active |
| Endoplus | 5375L | FDA UDI | Class II | Active |
| Endoplus | E308RR | FDA UDI | Class II | Active |
| Endoplus | E346MR-45 | FDA UDI | Class II | Active |
| Endoplus | 5365 | FDA UDI | Class II | Active |
| Endoplus | E313M | FDA UDI | Class II | Active |
| Endoplus | EN700 | FDA UDI | Class II | Active |
| Endoplus | E302RR-45 | FDA UDI | Class II | Active |
| Endoplus | EN309L | FDA UDI | Class II | Active |
Related Companies
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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. |