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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 5 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E382S | FDA UDI | Class II | Active |
| Endoplus | E333MR-45 | FDA UDI | Class II | Active |
| Endoplus | 5372L | FDA UDI | Class II | Active |
| Endoplus | E346SLR | FDA UDI | Class II | Active |
| Endoplus | 321VA | FDA UDI | Class II | Active |
| Endoplus | E331MR-25 | FDA UDI | Class II | Active |
| Endoplus | E346ACR-45 | FDA UDI | Class II | Active |
| Endoplus | E331M | FDA UDI | Class II | Active |
| Endoplus | 5MRC-43 | FDA UDI | Class II | Active |
| Endoplus | 5374 | FDA UDI | Class II | Active |
| Endoplus | 5300L | FDA UDI | Class II | Active |
| Endoplus | 5MFRRL | FDA UDI | Class II | Active |
| Endoplus | E333SR-45 | FDA UDI | Class II | Active |
| Endoplus | 5327 | FDA UDI | Class II | Active |
| Endoplus | E372MR | FDA UDI | Class II | Active |
| Endoplus | E322MR | FDA UDI | Class II | Active |
| Endoplus | 5344 | FDA UDI | Class II | Active |
| Endoplus | 365VA | FDA UDI | Class II | Active |
| Endoplus | 10431L | FDA UDI | Class II | Active |
| Endoplus | E338SLR | FDA UDI | Class II | Active |
| Endoplus | E327R-45 | FDA UDI | Class II | Active |
| Endoplus | 346VA | FDA UDI | Class II | Active |
| Endoplus | E420R | FDA UDI | Class II | Active |
| Endoplus | 5377J | FDA UDI | Class II | Active |
| Endoplus | 5MRCL | FDA UDI | Class II | Active |
| Endoplus | E312ACR | FDA UDI | Class II | Active |
| Endoplus | E329SLR-45 | FDA UDI | Class II | Active |
| Endoplus | 5349 | FDA UDI | Class II | Active |
| Endoplus | E325SR-45 | FDA UDI | Class II | Active |
| Endoplus | 5337L | FDA UDI | Class II | Active |
| Endoplus | E336SLR | FDA UDI | Class II | Active |
| Endoplus | 10432L | FDA UDI | Class II | Active |
| Endoplus | E370AC-45 | FDA UDI | Class II | Active |
| Endoplus | E338MR | FDA UDI | Class II | Active |
| Endoplus | E356SL | FDA UDI | Class II | Active |
| Endoplus | E335RR | FDA UDI | Class II | Active |
| Endoplus | E364SLR | FDA UDI | Class II | Active |
| Endoplus | E318SR | FDA UDI | Class II | Active |
| Endoplus | E304SLR-45 | FDA UDI | Class II | Active |
| Endoplus | 5337 | FDA UDI | Class II | Active |
| Endoplus | E345SLR-37 | FDA UDI | Class II | Active |
| Endoplus | 5396L | FDA UDI | Class II | Active |
| Endoplus | EN307L | FDA UDI | Class II | Active |
| Endoplus | E355MR | FDA UDI | Class II | Active |
| Endoplus | 364VA | FDA UDI | Class II | Active |
| Endoplus | 5320 | FDA UDI | Class II | Active |
| Endoplus | E300MR | FDA UDI | Class II | Active |
| Endoplus | 5304L | FDA UDI | Class II | Active |
| Endoplus | 5332 | FDA UDI | Class II | Active |
| Endoplus | E321R-45 | 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. |