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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 16 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E323SL | FDA UDI | Class II | Active |
| Endoplus | E324RR | FDA UDI | Class II | Active |
| Endoplus | E300RR-45 | FDA UDI | Class II | Active |
| Endoplus | E390DVR-45 | FDA UDI | Class II | Active |
| Endoplus | E349MR | FDA UDI | Class II | Active |
| Endoplus | 5RRL | FDA UDI | Class II | Active |
| Endoplus | E306M-45 | FDA UDI | Class II | Active |
| Endoplus | E420ACR-45 | FDA UDI | Class II | Active |
| Endoplus | 5393 | FDA UDI | Class II | Active |
| Endoplus | 321VL | FDA UDI | Class II | Active |
| Endoplus | E333ACR-45 | FDA UDI | Class II | Active |
| Endoplus | 5339 | FDA UDI | Class II | Active |
| Endoplus | E345RR | FDA UDI | Class II | Active |
| Endoplus | 302VA | FDA UDI | Class II | Active |
| Endoplus | E329RR | FDA UDI | Class II | Active |
| Endoplus | 5MRRC | FDA UDI | Class II | Active |
| Endoplus | 10R | FDA UDI | Class II | Active |
| Endoplus | 5751 | FDA UDI | Class II | Active |
| Endoplus | EN802L | FDA UDI | Class II | Active |
| Endoplus | 5327J | FDA UDI | Class II | Active |
| Endoplus | EN704 | FDA UDI | Class II | Active |
| Endoplus | E317SLR | FDA UDI | Class II | Active |
| Endoplus | E317ACR | FDA UDI | Class II | Active |
| Endoplus | E347ACR | FDA UDI | Class II | Active |
| Endoplus | 5340 | FDA UDI | Class II | Active |
| Endoplus | 5388 | FDA UDI | Class II | Active |
| Endoplus | E330RR-25 | FDA UDI | Class II | Active |
| Endoplus | E307R | FDA UDI | Class II | Active |
| Endoplus | E340R | FDA UDI | Class II | Active |
| Endoplus | E367DVR-45 | FDA UDI | Class II | Active |
| Endoplus | 5306 | FDA UDI | Class II | Active |
| Endoplus | E320M-45 | FDA UDI | Class II | Active |
| Endoplus | 5378 | FDA UDI | Class II | Active |
| Endoplus | E437S | FDA UDI | Class II | Active |
| Endoplus | E346DVR-45 | FDA UDI | Class II | Active |
| Endoplus | 5751L | FDA UDI | Class II | Active |
| Endoplus | ET333MR | FDA UDI | Class II | Active |
| Endoplus | E416S | FDA UDI | Class II | Active |
| Endoplus | E364RR-45 | FDA UDI | Class II | Active |
| Endoplus | 5SLFR | FDA UDI | Class II | Active |
| Endoplus | 5357 | FDA UDI | Class II | Active |
| Endoplus | 5551 | FDA UDI | Class II | Active |
| Endoplus | 5850L | FDA UDI | Class II | Active |
| Endoplus | E377SLR | FDA UDI | Class II | Active |
| Endoplus | SLRVA | FDA UDI | Class II | Active |
| Endoplus | 5319L | FDA UDI | Class II | Active |
| Endoplus | E364SR | FDA UDI | Class II | Active |
| Endoplus | E416SR | FDA UDI | Class II | Active |
| Endoplus | 5551L | FDA UDI | Class II | Active |
| Endoplus | E329SL | 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. |