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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 10 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E304R | FDA UDI | Class II | Active |
| Endoplus | 5334L | FDA UDI | Class II | Active |
| Endoplus | 333VL | FDA UDI | Class II | Active |
| Endoplus | 5301 | FDA UDI | Class II | Active |
| Endoplus | E306M | FDA UDI | Class II | Active |
| Endoplus | E322ACR | FDA UDI | Class II | Active |
| Endoplus | E390RR | FDA UDI | Class II | Active |
| Endoplus | 10437 | FDA UDI | Class II | Active |
| Endoplus | EN701 | FDA UDI | Class II | Active |
| Endoplus | E369MR-45 | FDA UDI | Class II | Active |
| Endoplus | 10416 | FDA UDI | Class II | Active |
| Endoplus | 5338L | FDA UDI | Class II | Active |
| Endoplus | 5364L | FDA UDI | Class II | Active |
| Endoplus | EN800 | FDA UDI | Class II | Active |
| Endoplus | 5398 | FDA UDI | Class II | Active |
| Endoplus | E420RR | FDA UDI | Class II | Active |
| Endoplus | 5373L | FDA UDI | Class II | Active |
| Endoplus | 10432 | FDA UDI | Class II | Active |
| Endoplus | E337RR | FDA UDI | Class II | Active |
| Endoplus | E327R | FDA UDI | Class II | Active |
| Endoplus | E326M | FDA UDI | Class II | Active |
| Endoplus | E333SL | FDA UDI | Class II | Active |
| Endoplus | E322SR | FDA UDI | Class II | Active |
| Endoplus | E355DVR | FDA UDI | Class II | Active |
| Endoplus | 5389L | FDA UDI | Class II | Active |
| Endoplus | E344SR | FDA UDI | Class II | Active |
| Endoplus | 369VA | FDA UDI | Class II | Active |
| Endoplus | E329MR-45 | FDA UDI | Class II | Active |
| Endoplus | E317MR-45 | FDA UDI | Class II | Active |
| Endoplus | E336MR | FDA UDI | Class II | Active |
| Endoplus | E327SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E306SLR | FDA UDI | Class II | Active |
| Endoplus | 5335 | FDA UDI | Class II | Active |
| Endoplus | E317MR | FDA UDI | Class II | Active |
| Endoplus | 5650 | FDA UDI | Class II | Active |
| Endoplus | E365MR-45 | FDA UDI | Class II | Active |
| Endoplus | EN320 | FDA UDI | Class II | Active |
| Endoplus | E309RR | FDA UDI | Class II | Active |
| Endoplus | 5304 | FDA UDI | Class II | Active |
| Endoplus | E346SR | FDA UDI | Class II | Active |
| Endoplus | E346ACR-37 | FDA UDI | Class II | Active |
| Endoplus | E333SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E313DVR | FDA UDI | Class II | Active |
| Endoplus | 10431 | FDA UDI | Class II | Active |
| Endoplus | E364ACR | FDA UDI | Class II | Active |
| Endoplus | E363RR-45 | FDA UDI | Class II | Active |
| Endoplus | 5550 | FDA UDI | Class II | Active |
| Endoplus | 5MRSJ | FDA UDI | Class II | Active |
| Endoplus | 10437L | FDA UDI | Class II | Active |
| Endoplus | E306MR-45 | 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. |