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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 4 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | 5MR | FDA UDI | Class II | Active |
| Endoplus | E337MR-45 | FDA UDI | Class II | Active |
| Endoplus | E365SLR | FDA UDI | Class II | Active |
| Endoplus | E374M | FDA UDI | Class II | Active |
| Endoplus | E437ACR | FDA UDI | Class II | Active |
| Endoplus | 5373 | FDA UDI | Class II | Active |
| Endoplus | EN700L | FDA UDI | Class II | Active |
| Endoplus | E434R | FDA UDI | Class II | Active |
| Endoplus | E319M | FDA UDI | Class II | Active |
| Endoplus | 5350L | FDA UDI | Class II | Active |
| Endoplus | 5388L | FDA UDI | Class II | Active |
| Endoplus | 5314 | FDA UDI | Class II | Active |
| Endoplus | EN307 | FDA UDI | Class II | Active |
| Endoplus | E416RR | FDA UDI | Class II | Active |
| Endoplus | E344SLR | FDA UDI | Class II | Active |
| Endoplus | E338SLR-45 | FDA UDI | Class II | Active |
| Endoplus | 5303L | FDA UDI | Class II | Active |
| Endoplus | 5382 | FDA UDI | Class II | Active |
| Endoplus | 5297L | FDA UDI | Class II | Active |
| Endoplus | E446RR | FDA UDI | Class II | Active |
| Endoplus | su5651J | FDA UDI | Class II | Active |
| Endoplus | E327MR-25 | FDA UDI | Class II | Active |
| Endoplus | 5332L | FDA UDI | Class II | Active |
| Endoplus | 5320L | FDA UDI | Class II | Active |
| Endoplus | 5329 | FDA UDI | Class II | Active |
| Endoplus | E341RR | FDA UDI | Class II | Active |
| Endoplus | E347R-25 | FDA UDI | Class II | Active |
| Endoplus | 347VA | FDA UDI | Class II | Active |
| Endoplus | 5333L | FDA UDI | Class II | Active |
| Endoplus | E437RR-45 | FDA UDI | Class II | Active |
| Endoplus | E342MR | FDA UDI | Class II | Active |
| Endoplus | 5329L | FDA UDI | Class II | Active |
| Endoplus | EN801 | FDA UDI | Class II | Active |
| Endoplus | E390SLR | FDA UDI | Class II | Active |
| Endoplus | 325VL | FDA UDI | Class II | Active |
| Endoplus | 5343 | FDA UDI | Class II | Active |
| Endoplus | E321AC | FDA UDI | Class II | Active |
| Endoplus | E347SLR | FDA UDI | Class II | Active |
| Endoplus | E313SR | FDA UDI | Class II | Active |
| Endoplus | E402SR | FDA UDI | Class II | Active |
| Endoplus | E375R | FDA UDI | Class II | Active |
| Endoplus | E349SR | FDA UDI | Class II | Active |
| Endoplus | E322DVR | FDA UDI | Class II | Active |
| Endoplus | E311MR | FDA UDI | Class II | Active |
| Endoplus | 5552L | FDA UDI | Class II | Active |
| Endoplus | 10MR | FDA UDI | Class II | Active |
| Endoplus | 5342 | FDA UDI | Class II | Active |
| Endoplus | E330RR-45 | FDA UDI | Class II | Active |
| Endoplus | E324RR-45 | FDA UDI | Class II | Active |
| Endoplus | EN703L | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
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Importers
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Notified Bodies
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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. |